Histiocytic Neoplasms, Version 2.2021, NCCN Clinical Practice Guidelines in Oncology
J Natl Compr Canc Netw. 2021 Nov;19(11):1277-1303. doi: 10.6004/jnccn.2021.0053.ABSTRACTHistiocytic neoplasms are rare hematologic disorders accounting for less than 1% of cancers of the soft tissue and lymph nodes. Clinical presentation and prognosis of these disorders can be highly variable, leading to challenges for diagnosis and optimal management of these patients. Treatment often consists of systemic therapy, and recent studies support use of targeted therapies for patients with these disorders. Observation ("watch and wait") may be sufficient for select patients with mild disease. These NCCN Guidelines for...
Source: Journal of the National Comprehensive Cancer Network : JNCCN - November 15, 2021 Category: Cancer & Oncology Authors: Ronald S Go Eric Jacobsen Robert Baiocchi Ilia Buhtoiarov Erin B Butler Patrick K Campbell Don W Coulter Eli Diamond Aron Flagg Aaron M Goodman Gaurav Goyal Dita Gratzinger Paul C Hendrie Meghan Higman Michael D Hogarty Filip Janku Reem Karmali David Morg Source Type: research

Challenges in the Histopathologic Diagnosis of Histiocytic Neoplasms
J Natl Compr Canc Netw. 2021 Nov;19(11):1305-1311. doi: 10.6004/jnccn.2021.7098.ABSTRACTHistiocytic neoplasms, including Langerhans cell histiocytosis (LCH), Erdheim-Chester disease (ECD), and Rosai-Dorfman disease (RDD), present a diagnostic challenge due to nonspecific fibroinflammatory infiltrates and a diverse clinical presentation. The pathologist can play a key role in classification of these disorders through multidisciplinary collaboration and correlation of pathologic features with clinical and radiologic findings. The histopathologic differential diagnosis is broad, requiring knowledge of the possible diagnoses a...
Source: Journal of the National Comprehensive Cancer Network : JNCCN - November 15, 2021 Category: Cancer & Oncology Authors: Karen L Rech Rong He Source Type: research

Histiocytic Neoplasms, Version 2.2021, NCCN Clinical Practice Guidelines in Oncology
J Natl Compr Canc Netw. 2021 Nov;19(11):1277-1303. doi: 10.6004/jnccn.2021.0053.ABSTRACTHistiocytic neoplasms are rare hematologic disorders accounting for less than 1% of cancers of the soft tissue and lymph nodes. Clinical presentation and prognosis of these disorders can be highly variable, leading to challenges for diagnosis and optimal management of these patients. Treatment often consists of systemic therapy, and recent studies support use of targeted therapies for patients with these disorders. Observation ("watch and wait") may be sufficient for select patients with mild disease. These NCCN Guidelines for...
Source: Journal of the National Comprehensive Cancer Network : JNCCN - November 15, 2021 Category: Cancer & Oncology Authors: Ronald S Go Eric Jacobsen Robert Baiocchi Ilia Buhtoiarov Erin B Butler Patrick K Campbell Don W Coulter Eli Diamond Aron Flagg Aaron M Goodman Gaurav Goyal Dita Gratzinger Paul C Hendrie Meghan Higman Michael D Hogarty Filip Janku Reem Karmali David Morg Source Type: research

Survivorship Issues in Adult Patients With Histiocytic Neoplasms
J Natl Compr Canc Netw. 2021 Nov;19(11):1312-1318. doi: 10.6004/jnccn.2021.7096.ABSTRACTAdult-onset histiocytoses (AOH), primarily Rosai-Dorfman disease (RDD), Erdheim-Chester Disease (ECD), and adult Langerhans cell histiocytosis (ALCH), are a group of related histiocytic neoplastic disorders featuring multisystemic manifestations. The disorders are largely incurable, and are essentially chronic neoplastic diseases with a variable prognosis. Prompt diagnosis and treatment is important to prevent debilitating and even life-threatening complications. Survivorship issues abound in AOH, due to their multisystemic manifestatio...
Source: Journal of the National Comprehensive Cancer Network : JNCCN - November 15, 2021 Category: Cancer & Oncology Authors: Kevin O'Brien Rahul Dave Skand Shekhar Fady Hannah-Shmouni Leora E Comis Beth I Solomon Marcus Chen William A Gahl Edmond FitzGibbon Bernadette R Gochuico Juvianee I Estrada-Veras Source Type: research

Challenges in the Histopathologic Diagnosis of Histiocytic Neoplasms
J Natl Compr Canc Netw. 2021 Nov;19(11):1305-1311. doi: 10.6004/jnccn.2021.7098.ABSTRACTHistiocytic neoplasms, including Langerhans cell histiocytosis (LCH), Erdheim-Chester disease (ECD), and Rosai-Dorfman disease (RDD), present a diagnostic challenge due to nonspecific fibroinflammatory infiltrates and a diverse clinical presentation. The pathologist can play a key role in classification of these disorders through multidisciplinary collaboration and correlation of pathologic features with clinical and radiologic findings. The histopathologic differential diagnosis is broad, requiring knowledge of the possible diagnoses a...
Source: Journal of the National Comprehensive Cancer Network : JNCCN - November 15, 2021 Category: Cancer & Oncology Authors: Karen L Rech Rong He Source Type: research

Survivorship Issues in Adult Patients With Histiocytic Neoplasms
J Natl Compr Canc Netw. 2021 Nov;19(11):1312-1318. doi: 10.6004/jnccn.2021.7096.ABSTRACTAdult-onset histiocytoses (AOH), primarily Rosai-Dorfman disease (RDD), Erdheim-Chester Disease (ECD), and adult Langerhans cell histiocytosis (ALCH), are a group of related histiocytic neoplastic disorders featuring multisystemic manifestations. The disorders are largely incurable, and are essentially chronic neoplastic diseases with a variable prognosis. Prompt diagnosis and treatment is important to prevent debilitating and even life-threatening complications. Survivorship issues abound in AOH, due to their multisystemic manifestatio...
Source: Journal of the National Comprehensive Cancer Network : JNCCN - November 15, 2021 Category: Cancer & Oncology Authors: Kevin O'Brien Rahul Dave Skand Shekhar Fady Hannah-Shmouni Leora E Comis Beth I Solomon Marcus Chen William A Gahl Edmond FitzGibbon Bernadette R Gochuico Juvianee I Estrada-Veras Source Type: research

Challenges in the Histopathologic Diagnosis of Histiocytic Neoplasms
J Natl Compr Canc Netw. 2021 Nov;19(11):1305-1311. doi: 10.6004/jnccn.2021.7098.ABSTRACTHistiocytic neoplasms, including Langerhans cell histiocytosis (LCH), Erdheim-Chester disease (ECD), and Rosai-Dorfman disease (RDD), present a diagnostic challenge due to nonspecific fibroinflammatory infiltrates and a diverse clinical presentation. The pathologist can play a key role in classification of these disorders through multidisciplinary collaboration and correlation of pathologic features with clinical and radiologic findings. The histopathologic differential diagnosis is broad, requiring knowledge of the possible diagnoses a...
Source: Journal of the National Comprehensive Cancer Network : JNCCN - November 15, 2021 Category: Cancer & Oncology Authors: Karen L Rech Rong He Source Type: research

Histiocytic Neoplasms, Version 2.2021, NCCN Clinical Practice Guidelines in Oncology
J Natl Compr Canc Netw. 2021 Nov;19(11):1277-1303. doi: 10.6004/jnccn.2021.0053.ABSTRACTHistiocytic neoplasms are rare hematologic disorders accounting for less than 1% of cancers of the soft tissue and lymph nodes. Clinical presentation and prognosis of these disorders can be highly variable, leading to challenges for diagnosis and optimal management of these patients. Treatment often consists of systemic therapy, and recent studies support use of targeted therapies for patients with these disorders. Observation ("watch and wait") may be sufficient for select patients with mild disease. These NCCN Guidelines for...
Source: Journal of the National Comprehensive Cancer Network : JNCCN - November 15, 2021 Category: Cancer & Oncology Authors: Ronald S Go Eric Jacobsen Robert Baiocchi Ilia Buhtoiarov Erin B Butler Patrick K Campbell Don W Coulter Eli Diamond Aron Flagg Aaron M Goodman Gaurav Goyal Dita Gratzinger Paul C Hendrie Meghan Higman Michael D Hogarty Filip Janku Reem Karmali David Morg Source Type: research

Survivorship Issues in Adult Patients With Histiocytic Neoplasms
J Natl Compr Canc Netw. 2021 Nov;19(11):1312-1318. doi: 10.6004/jnccn.2021.7096.ABSTRACTAdult-onset histiocytoses (AOH), primarily Rosai-Dorfman disease (RDD), Erdheim-Chester Disease (ECD), and adult Langerhans cell histiocytosis (ALCH), are a group of related histiocytic neoplastic disorders featuring multisystemic manifestations. The disorders are largely incurable, and are essentially chronic neoplastic diseases with a variable prognosis. Prompt diagnosis and treatment is important to prevent debilitating and even life-threatening complications. Survivorship issues abound in AOH, due to their multisystemic manifestatio...
Source: Journal of the National Comprehensive Cancer Network : JNCCN - November 15, 2021 Category: Cancer & Oncology Authors: Kevin O'Brien Rahul Dave Skand Shekhar Fady Hannah-Shmouni Leora E Comis Beth I Solomon Marcus Chen William A Gahl Edmond FitzGibbon Bernadette R Gochuico Juvianee I Estrada-Veras Source Type: research

Rosai-Dorfman disease of thymus with elevated serum anti-acetylcholine receptor antibody: a case report
We examined the relationship between Rosai-Dorfman disease and elevated anti-acetylcholine receptor antibody. To our knowledge, elevated anti-acetylcholine receptor antibody has not been reported in isolated thymic Rosai-Dorfman disease.PMID:34760043 | PMC:PMC8569306 (Source: International Journal of Clinical and Experimental Pathology)
Source: International Journal of Clinical and Experimental Pathology - November 11, 2021 Category: Pathology Authors: Ryusuke Tsujimura Daisuke Sato Hiyo Obikane Riken Kawachi Masahiko Sugitani Hiroyuki Hao Hiroyuki Sakurai Mitsunori Yamakawa Shinobu Masuda Source Type: research

Rosai-Dorfman disease of thymus with elevated serum anti-acetylcholine receptor antibody: a case report
We examined the relationship between Rosai-Dorfman disease and elevated anti-acetylcholine receptor antibody. To our knowledge, elevated anti-acetylcholine receptor antibody has not been reported in isolated thymic Rosai-Dorfman disease.PMID:34760043 | PMC:PMC8569306 (Source: International Journal of Clinical and Experimental Pathology)
Source: International Journal of Clinical and Experimental Pathology - November 11, 2021 Category: Pathology Authors: Ryusuke Tsujimura Daisuke Sato Hiyo Obikane Riken Kawachi Masahiko Sugitani Hiroyuki Hao Hiroyuki Sakurai Mitsunori Yamakawa Shinobu Masuda Source Type: research

Rosai-Dorfman disease of thymus with elevated serum anti-acetylcholine receptor antibody: a case report
We examined the relationship between Rosai-Dorfman disease and elevated anti-acetylcholine receptor antibody. To our knowledge, elevated anti-acetylcholine receptor antibody has not been reported in isolated thymic Rosai-Dorfman disease.PMID:34760043 | PMC:PMC8569306 (Source: International Journal of Clinical and Experimental Pathology)
Source: International Journal of Clinical and Experimental Pathology - November 11, 2021 Category: Pathology Authors: Ryusuke Tsujimura Daisuke Sato Hiyo Obikane Riken Kawachi Masahiko Sugitani Hiroyuki Hao Hiroyuki Sakurai Mitsunori Yamakawa Shinobu Masuda Source Type: research

Rosai-Dorfman disease of thymus with elevated serum anti-acetylcholine receptor antibody: a case report
We examined the relationship between Rosai-Dorfman disease and elevated anti-acetylcholine receptor antibody. To our knowledge, elevated anti-acetylcholine receptor antibody has not been reported in isolated thymic Rosai-Dorfman disease.PMID:34760043 | PMC:PMC8569306 (Source: International Journal of Clinical and Experimental Pathology)
Source: International Journal of Clinical and Experimental Pathology - November 11, 2021 Category: Pathology Authors: Ryusuke Tsujimura Daisuke Sato Hiyo Obikane Riken Kawachi Masahiko Sugitani Hiroyuki Hao Hiroyuki Sakurai Mitsunori Yamakawa Shinobu Masuda Source Type: research

Rosai-Dorfman disease of thymus with elevated serum anti-acetylcholine receptor antibody: a case report
We examined the relationship between Rosai-Dorfman disease and elevated anti-acetylcholine receptor antibody. To our knowledge, elevated anti-acetylcholine receptor antibody has not been reported in isolated thymic Rosai-Dorfman disease.PMID:34760043 | PMC:PMC8569306 (Source: International Journal of Clinical and Experimental Pathology)
Source: International Journal of Clinical and Experimental Pathology - November 11, 2021 Category: Pathology Authors: Ryusuke Tsujimura Daisuke Sato Hiyo Obikane Riken Kawachi Masahiko Sugitani Hiroyuki Hao Hiroyuki Sakurai Mitsunori Yamakawa Shinobu Masuda Source Type: research

Rosai-Dorfman disease of thymus with elevated serum anti-acetylcholine receptor antibody: a case report
We examined the relationship between Rosai-Dorfman disease and elevated anti-acetylcholine receptor antibody. To our knowledge, elevated anti-acetylcholine receptor antibody has not been reported in isolated thymic Rosai-Dorfman disease.PMID:34760043 | PMC:PMC8569306 (Source: International Journal of Clinical and Experimental Pathology)
Source: International Journal of Clinical and Experimental Pathology - November 11, 2021 Category: Pathology Authors: Ryusuke Tsujimura Daisuke Sato Hiyo Obikane Riken Kawachi Masahiko Sugitani Hiroyuki Hao Hiroyuki Sakurai Mitsunori Yamakawa Shinobu Masuda Source Type: research

Rosai-Dorfman disease of thymus with elevated serum anti-acetylcholine receptor antibody: a case report
We examined the relationship between Rosai-Dorfman disease and elevated anti-acetylcholine receptor antibody. To our knowledge, elevated anti-acetylcholine receptor antibody has not been reported in isolated thymic Rosai-Dorfman disease.PMID:34760043 | PMC:PMC8569306 (Source: International Journal of Clinical and Experimental Pathology)
Source: International Journal of Clinical and Experimental Pathology - November 11, 2021 Category: Pathology Authors: Ryusuke Tsujimura Daisuke Sato Hiyo Obikane Riken Kawachi Masahiko Sugitani Hiroyuki Hao Hiroyuki Sakurai Mitsunori Yamakawa Shinobu Masuda Source Type: research

Rosai-Dorfman disease of thymus with elevated serum anti-acetylcholine receptor antibody: a case report
We examined the relationship between Rosai-Dorfman disease and elevated anti-acetylcholine receptor antibody. To our knowledge, elevated anti-acetylcholine receptor antibody has not been reported in isolated thymic Rosai-Dorfman disease.PMID:34760043 | PMC:PMC8569306 (Source: International Journal of Clinical and Experimental Pathology)
Source: International Journal of Clinical and Experimental Pathology - November 11, 2021 Category: Pathology Authors: Ryusuke Tsujimura Daisuke Sato Hiyo Obikane Riken Kawachi Masahiko Sugitani Hiroyuki Hao Hiroyuki Sakurai Mitsunori Yamakawa Shinobu Masuda Source Type: research

Rosai-Dorfman disease of thymus with elevated serum anti-acetylcholine receptor antibody: a case report
We examined the relationship between Rosai-Dorfman disease and elevated anti-acetylcholine receptor antibody. To our knowledge, elevated anti-acetylcholine receptor antibody has not been reported in isolated thymic Rosai-Dorfman disease.PMID:34760043 | PMC:PMC8569306 (Source: International Journal of Clinical and Experimental Pathology)
Source: International Journal of Clinical and Experimental Pathology - November 11, 2021 Category: Pathology Authors: Ryusuke Tsujimura Daisuke Sato Hiyo Obikane Riken Kawachi Masahiko Sugitani Hiroyuki Hao Hiroyuki Sakurai Mitsunori Yamakawa Shinobu Masuda Source Type: research

Rosai-Dorfman disease of thymus with elevated serum anti-acetylcholine receptor antibody: a case report
We examined the relationship between Rosai-Dorfman disease and elevated anti-acetylcholine receptor antibody. To our knowledge, elevated anti-acetylcholine receptor antibody has not been reported in isolated thymic Rosai-Dorfman disease.PMID:34760043 | PMC:PMC8569306 (Source: International Journal of Clinical and Experimental Pathology)
Source: International Journal of Clinical and Experimental Pathology - November 11, 2021 Category: Pathology Authors: Ryusuke Tsujimura Daisuke Sato Hiyo Obikane Riken Kawachi Masahiko Sugitani Hiroyuki Hao Hiroyuki Sakurai Mitsunori Yamakawa Shinobu Masuda Source Type: research

Rosai-Dorfman disease of thymus with elevated serum anti-acetylcholine receptor antibody: a case report
We examined the relationship between Rosai-Dorfman disease and elevated anti-acetylcholine receptor antibody. To our knowledge, elevated anti-acetylcholine receptor antibody has not been reported in isolated thymic Rosai-Dorfman disease.PMID:34760043 | PMC:PMC8569306 (Source: International Journal of Clinical and Experimental Pathology)
Source: International Journal of Clinical and Experimental Pathology - November 11, 2021 Category: Pathology Authors: Ryusuke Tsujimura Daisuke Sato Hiyo Obikane Riken Kawachi Masahiko Sugitani Hiroyuki Hao Hiroyuki Sakurai Mitsunori Yamakawa Shinobu Masuda Source Type: research

Is it Anaplastic Thyroid Cancer, Primary Thyroid Lymphoma, or Rosai Dorfman Disease? An Elusive Histopathologic Diagnosis of a Thyroid Mass
AbstractThe aim of this study is to present an elusive case of primary thyroid lymphoma (PTL), initially thought to be anaplastic thyroid carcinoma, then Rosai Dorfman disease, before the final diagnosis of PTL was made.  An elderly female with hypothyroidism presented with compressive airway symptoms secondary to an enlarging neck mass. Imaging was suggestive of undifferentiated thyroid cancer. The initial biopsy was unexpectedly consistent with a lymphoproliferative disorder such as Rosai-Dorfman disease. A repea t biopsy with immunohistochemical analysis yielded a diagnosis of diffuse large B-cell lymphoma of germi...
Source: Head and Neck Pathology - November 9, 2021 Category: Pathology Source Type: research

Successful treatment of multisystemic Rosai-Dorfman disease with lenalidomide and dexamethasone: a case report
(Source: Annals of Hematology)
Source: Annals of Hematology - November 6, 2021 Category: Hematology Source Type: research

Ophthalmic histiocytic lesions: a baseline demographic and clinicopathological study of 28 cases from two eye centers
ConclusionsHistiocytic disease is more likely to be overlooked clinically owing to its rarity. In the C group, juvenile xanthogranuloma (JXG) was the most commonly encountered histiocytic lesion and had a tendency to present at a later age with extremely rare intraocular involvement in contrast to previously published reports. The median age at presentation was higher in group R. All patients in group L had strictly unilateral disease, while RDD (group R) was most commonly bilateral. Future research on genetic aspects, management, and prognosis is necessary. (Source: International Ophthalmology)
Source: International Ophthalmology - November 2, 2021 Category: Opthalmology Source Type: research

A Rare Case Report of Rosai-Dorfman Disease Manifesting as a Mediastinal Mass
No abstract available (Source: Journal of Thoracic Imaging)
Source: Journal of Thoracic Imaging - October 28, 2021 Category: Radiology Tags: Web Exclusive Content: JSTR Meeting Notes Source Type: research

Bilateral Ocular Rosai-Dorfman Disease Presenting as Diffuse Anterior Scleritis with Multiple Enlarging Epibulbar Masses
CONCLUSIONS: Rosai-Dorfman disease can present as bilateral scleritis initially and develop epibulbar masses without any systemic involvement. Biopsy with immunohistochemical analysis can aid in the diagnosis.PMID:34662245 | DOI:10.1080/09273948.2021.1986547 (Source: Ocular Immunology and Inflammation)
Source: Ocular Immunology and Inflammation - October 18, 2021 Category: Allergy & Immunology Authors: Mamta Agarwal Gayatri S Geetha Iyer Subramanian KrishnaKumar Emmett T Cunningham Source Type: research

Rosai-Dorfman disease of the lumbar region: A case report
Asian J Surg. 2021 Oct 8:S1015-9584(21)00563-7. doi: 10.1016/j.asjsur.2021.08.060. Online ahead of print.NO ABSTRACTPMID:34635408 | DOI:10.1016/j.asjsur.2021.08.060 (Source: Asian Journal of Surgery)
Source: Asian Journal of Surgery - October 12, 2021 Category: Surgery Authors: Xiaoxuan Zhou Rui Zhang Jie He Hongjie Hu Source Type: research

Acute Tubulointerstitial Nephritis in Rosai-Dorfman Disease Mimicking IgG4-related Disease
Intern Med. 2021 Sep 18. doi: 10.2169/internalmedicine.8046-21. Online ahead of print.ABSTRACTRosai-Dorfman-Destombes disease (RDD) is a non-Langerhans cell histiocytosis characterized by the accumulation of histiocytes inside the lymph nodes or extranodally. The association between RDD and IgG4-related disease (IgG4-RD) is discussed. We herein report a case of RDD manifesting as acute tubulointerstitial nephritis mimicking IgG4-RD. The first renal biopsy showed severe tubulointerstitial nephritis with infiltration of S100-positive histiocytes and IgG4-positive plasma cells; storiform fibrosis and obliterative phlebitis we...
Source: Internal Medicine - September 21, 2021 Category: Internal Medicine Authors: Satoshi Kurahashi Naohiro Toda Masaaki Fujita Katsuya Tanigaki Jun Takeoka Hisako Hirashima Eri Muso Katsuhiro Io Takaki Sakurai Toshiyuki Komiya Source Type: research

Rosai ‐Dorfman disease in 6‐year‐old child: Presentation, diagnosis, and treatment
Rosai-Dorfman disease is referred to as sinus histiocytosis massive lymphadenopathy. We are reporting a rare case of Rosai-Dorfman disease, a case of 6-year-old boy with a history of multiple painless submandibular and cervical lymphadenopathy. AbstractRosai-Dorfman disease is referred to as sinus histiocytosis massive lymphadenopathy. We are reporting a rare case of Rosai-Dorfman disease, a case of 6-year-old boy with a history of multiple painless submandibular and cervical lymphadenopathy. (Source: Clinical Case Reports)
Source: Clinical Case Reports - September 21, 2021 Category: General Medicine Authors: Kalpana Giri, Ashok Baral, Niva Tiwari, Krishna Sagar Sharma Tags: CASE REPORT Source Type: research

Rosai-Dorfman disease in the central nervous system with two isolated lesions originated from a single clone: a case report
Rosai –Dorfman disease (RDD) is a rare, benign, idiopathic non-Langerhans cell histiocytosis. Cases of RDD in the CNS are extremely rare but lethal. RDD is thought to represent a reactive process. Recent studie... (Source: BMC Neurology)
Source: BMC Neurology - September 13, 2021 Category: Neurology Authors: Huawei Jin, Zhenhua Yu, Tian Tian, Guoping Shen, Weian Chen, Miao Fan, Qun He, Fei Xu and Dawei Liu Tags: Case report Source Type: research

Rosai ‐Dorfman disease presenting with solitary liver mass without lymphadenopathy: A case report
Rosai-Dorfman disease (RDD), as a lymphoproliferative disorder with unknown etiology, is commonly identified with systemic clinical manifestations in various organs. In this case study, RDD occurrence was reported with an exceedingly liver mass. AbstractRosai-Dorfman disease (RDD), as a lymphoproliferative disorder with unknown etiology, is commonly identified with systemic clinical manifestations in various organs. In this case study, RDD occurrence was reported with an exceedingly liver mass. (Source: Clinical Case Reports)
Source: Clinical Case Reports - August 25, 2021 Category: General Medicine Authors: Yousef Roosta, Ali Esfahani, Amir Vahedi, Kosar Tarvirizadeh, Sadegh Asoubar, Behdad Boroofeh, Roshan Dinparast, Farhad Behzadi, Mortaza Raeisi, Mohammadreza Mohammad Hosseiniazar Tags: CASE REPORT Source Type: research

Musculoskeletal imaging features of non-Langerhans cell histiocytoses
This article reviews the musculoskeletal imaging appearances of the commoner N-LCH. (Source: Skeletal Radiology)
Source: Skeletal Radiology - August 15, 2021 Category: Radiology Source Type: research

Intracranial Rosai-Dorfman disease mimicking isolated meningioma: a case report and review of the literature
Int J Clin Exp Pathol. 2021 Jul 15;14(7):827-830. eCollection 2021.ABSTRACTRosai-Dorfman disease is a rare malignant infirmity. Here, we present a case of a 57-year-old man with giddiness and unstable gait, as well as blurred vision in the left eye for four months. Radiologically the diagnosis before surgery was meningioma. The patient received a craniotomy, and the histopathologic diagnosis was Rosai-Dorfman disease. We reviewed the diagnosis, mechanism, and treatment of this disease.PMID:34367414 | PMC:PMC8339718 (Source: International Journal of Clinical and Experimental Pathology)
Source: International Journal of Clinical and Experimental Pathology - August 9, 2021 Category: Pathology Authors: Lin Xia Li Zhang Yue Xiang Liping Liu Zonglin Jing Source Type: research

Intracranial Rosai-Dorfman disease mimicking isolated meningioma: a case report and review of the literature
Int J Clin Exp Pathol. 2021 Jul 15;14(7):827-830. eCollection 2021.ABSTRACTRosai-Dorfman disease is a rare malignant infirmity. Here, we present a case of a 57-year-old man with giddiness and unstable gait, as well as blurred vision in the left eye for four months. Radiologically the diagnosis before surgery was meningioma. The patient received a craniotomy, and the histopathologic diagnosis was Rosai-Dorfman disease. We reviewed the diagnosis, mechanism, and treatment of this disease.PMID:34367414 | PMC:PMC8339718 (Source: International Journal of Clinical and Experimental Pathology)
Source: International Journal of Clinical and Experimental Pathology - August 9, 2021 Category: Pathology Authors: Lin Xia Li Zhang Yue Xiang Liping Liu Zonglin Jing Source Type: research

Intracranial Rosai-Dorfman disease mimicking isolated meningioma: a case report and review of the literature
Int J Clin Exp Pathol. 2021 Jul 15;14(7):827-830. eCollection 2021.ABSTRACTRosai-Dorfman disease is a rare malignant infirmity. Here, we present a case of a 57-year-old man with giddiness and unstable gait, as well as blurred vision in the left eye for four months. Radiologically the diagnosis before surgery was meningioma. The patient received a craniotomy, and the histopathologic diagnosis was Rosai-Dorfman disease. We reviewed the diagnosis, mechanism, and treatment of this disease.PMID:34367414 | PMC:PMC8339718 (Source: International Journal of Clinical and Experimental Pathology)
Source: International Journal of Clinical and Experimental Pathology - August 9, 2021 Category: Pathology Authors: Lin Xia Li Zhang Yue Xiang Liping Liu Zonglin Jing Source Type: research

Intracranial Rosai-Dorfman disease mimicking isolated meningioma: a case report and review of the literature
Int J Clin Exp Pathol. 2021 Jul 15;14(7):827-830. eCollection 2021.ABSTRACTRosai-Dorfman disease is a rare malignant infirmity. Here, we present a case of a 57-year-old man with giddiness and unstable gait, as well as blurred vision in the left eye for four months. Radiologically the diagnosis before surgery was meningioma. The patient received a craniotomy, and the histopathologic diagnosis was Rosai-Dorfman disease. We reviewed the diagnosis, mechanism, and treatment of this disease.PMID:34367414 | PMC:PMC8339718 (Source: International Journal of Clinical and Experimental Pathology)
Source: International Journal of Clinical and Experimental Pathology - August 9, 2021 Category: Pathology Authors: Lin Xia Li Zhang Yue Xiang Liping Liu Zonglin Jing Source Type: research

Intracranial Rosai-Dorfman disease mimicking isolated meningioma: a case report and review of the literature
Int J Clin Exp Pathol. 2021 Jul 15;14(7):827-830. eCollection 2021.ABSTRACTRosai-Dorfman disease is a rare malignant infirmity. Here, we present a case of a 57-year-old man with giddiness and unstable gait, as well as blurred vision in the left eye for four months. Radiologically the diagnosis before surgery was meningioma. The patient received a craniotomy, and the histopathologic diagnosis was Rosai-Dorfman disease. We reviewed the diagnosis, mechanism, and treatment of this disease.PMID:34367414 | PMC:PMC8339718 (Source: International Journal of Clinical and Experimental Pathology)
Source: International Journal of Clinical and Experimental Pathology - August 9, 2021 Category: Pathology Authors: Lin Xia Li Zhang Yue Xiang Liping Liu Zonglin Jing Source Type: research

Intracranial Rosai-Dorfman disease mimicking isolated meningioma: a case report and review of the literature
Int J Clin Exp Pathol. 2021 Jul 15;14(7):827-830. eCollection 2021.ABSTRACTRosai-Dorfman disease is a rare malignant infirmity. Here, we present a case of a 57-year-old man with giddiness and unstable gait, as well as blurred vision in the left eye for four months. Radiologically the diagnosis before surgery was meningioma. The patient received a craniotomy, and the histopathologic diagnosis was Rosai-Dorfman disease. We reviewed the diagnosis, mechanism, and treatment of this disease.PMID:34367414 | PMC:PMC8339718 (Source: International Journal of Clinical and Experimental Pathology)
Source: International Journal of Clinical and Experimental Pathology - August 9, 2021 Category: Pathology Authors: Lin Xia Li Zhang Yue Xiang Liping Liu Zonglin Jing Source Type: research

Intracranial Rosai-Dorfman disease mimicking isolated meningioma: a case report and review of the literature
Int J Clin Exp Pathol. 2021 Jul 15;14(7):827-830. eCollection 2021.ABSTRACTRosai-Dorfman disease is a rare malignant infirmity. Here, we present a case of a 57-year-old man with giddiness and unstable gait, as well as blurred vision in the left eye for four months. Radiologically the diagnosis before surgery was meningioma. The patient received a craniotomy, and the histopathologic diagnosis was Rosai-Dorfman disease. We reviewed the diagnosis, mechanism, and treatment of this disease.PMID:34367414 | PMC:PMC8339718 (Source: International Journal of Clinical and Experimental Pathology)
Source: International Journal of Clinical and Experimental Pathology - August 9, 2021 Category: Pathology Authors: Lin Xia Li Zhang Yue Xiang Liping Liu Zonglin Jing Source Type: research

Intracranial Rosai-Dorfman disease mimicking isolated meningioma: a case report and review of the literature
Int J Clin Exp Pathol. 2021 Jul 15;14(7):827-830. eCollection 2021.ABSTRACTRosai-Dorfman disease is a rare malignant infirmity. Here, we present a case of a 57-year-old man with giddiness and unstable gait, as well as blurred vision in the left eye for four months. Radiologically the diagnosis before surgery was meningioma. The patient received a craniotomy, and the histopathologic diagnosis was Rosai-Dorfman disease. We reviewed the diagnosis, mechanism, and treatment of this disease.PMID:34367414 | PMC:PMC8339718 (Source: International Journal of Clinical and Experimental Pathology)
Source: International Journal of Clinical and Experimental Pathology - August 9, 2021 Category: Pathology Authors: Lin Xia Li Zhang Yue Xiang Liping Liu Zonglin Jing Source Type: research

Intracranial Rosai-Dorfman disease mimicking isolated meningioma: a case report and review of the literature
Int J Clin Exp Pathol. 2021 Jul 15;14(7):827-830. eCollection 2021.ABSTRACTRosai-Dorfman disease is a rare malignant infirmity. Here, we present a case of a 57-year-old man with giddiness and unstable gait, as well as blurred vision in the left eye for four months. Radiologically the diagnosis before surgery was meningioma. The patient received a craniotomy, and the histopathologic diagnosis was Rosai-Dorfman disease. We reviewed the diagnosis, mechanism, and treatment of this disease.PMID:34367414 | PMC:PMC8339718 (Source: International Journal of Clinical and Experimental Pathology)
Source: International Journal of Clinical and Experimental Pathology - August 9, 2021 Category: Pathology Authors: Lin Xia Li Zhang Yue Xiang Liping Liu Zonglin Jing Source Type: research

Intracranial Rosai-Dorfman disease mimicking isolated meningioma: a case report and review of the literature
Int J Clin Exp Pathol. 2021 Jul 15;14(7):827-830. eCollection 2021.ABSTRACTRosai-Dorfman disease is a rare malignant infirmity. Here, we present a case of a 57-year-old man with giddiness and unstable gait, as well as blurred vision in the left eye for four months. Radiologically the diagnosis before surgery was meningioma. The patient received a craniotomy, and the histopathologic diagnosis was Rosai-Dorfman disease. We reviewed the diagnosis, mechanism, and treatment of this disease.PMID:34367414 | PMC:PMC8339718 (Source: International Journal of Clinical and Experimental Pathology)
Source: International Journal of Clinical and Experimental Pathology - August 9, 2021 Category: Pathology Authors: Lin Xia Li Zhang Yue Xiang Liping Liu Zonglin Jing Source Type: research

Intracranial Rosai-Dorfman disease mimicking isolated meningioma: a case report and review of the literature
Int J Clin Exp Pathol. 2021 Jul 15;14(7):827-830. eCollection 2021.ABSTRACTRosai-Dorfman disease is a rare malignant infirmity. Here, we present a case of a 57-year-old man with giddiness and unstable gait, as well as blurred vision in the left eye for four months. Radiologically the diagnosis before surgery was meningioma. The patient received a craniotomy, and the histopathologic diagnosis was Rosai-Dorfman disease. We reviewed the diagnosis, mechanism, and treatment of this disease.PMID:34367414 | PMC:PMC8339718 (Source: International Journal of Clinical and Experimental Pathology)
Source: International Journal of Clinical and Experimental Pathology - August 9, 2021 Category: Pathology Authors: Lin Xia Li Zhang Yue Xiang Liping Liu Zonglin Jing Source Type: research

Intracranial Rosai-Dorfman disease mimicking isolated meningioma: a case report and review of the literature
Int J Clin Exp Pathol. 2021 Jul 15;14(7):827-830. eCollection 2021.ABSTRACTRosai-Dorfman disease is a rare malignant infirmity. Here, we present a case of a 57-year-old man with giddiness and unstable gait, as well as blurred vision in the left eye for four months. Radiologically the diagnosis before surgery was meningioma. The patient received a craniotomy, and the histopathologic diagnosis was Rosai-Dorfman disease. We reviewed the diagnosis, mechanism, and treatment of this disease.PMID:34367414 | PMC:PMC8339718 (Source: International Journal of Clinical and Experimental Pathology)
Source: International Journal of Clinical and Experimental Pathology - August 9, 2021 Category: Pathology Authors: Lin Xia Li Zhang Yue Xiang Liping Liu Zonglin Jing Source Type: research

Intracranial Rosai-Dorfman disease mimicking isolated meningioma: a case report and review of the literature
Int J Clin Exp Pathol. 2021 Jul 15;14(7):827-830. eCollection 2021.ABSTRACTRosai-Dorfman disease is a rare malignant infirmity. Here, we present a case of a 57-year-old man with giddiness and unstable gait, as well as blurred vision in the left eye for four months. Radiologically the diagnosis before surgery was meningioma. The patient received a craniotomy, and the histopathologic diagnosis was Rosai-Dorfman disease. We reviewed the diagnosis, mechanism, and treatment of this disease.PMID:34367414 | PMC:PMC8339718 (Source: International Journal of Clinical and Experimental Pathology)
Source: International Journal of Clinical and Experimental Pathology - August 9, 2021 Category: Pathology Authors: Lin Xia Li Zhang Yue Xiang Liping Liu Zonglin Jing Source Type: research

Intracranial Rosai-Dorfman disease mimicking isolated meningioma: a case report and review of the literature
Int J Clin Exp Pathol. 2021 Jul 15;14(7):827-830. eCollection 2021.ABSTRACTRosai-Dorfman disease is a rare malignant infirmity. Here, we present a case of a 57-year-old man with giddiness and unstable gait, as well as blurred vision in the left eye for four months. Radiologically the diagnosis before surgery was meningioma. The patient received a craniotomy, and the histopathologic diagnosis was Rosai-Dorfman disease. We reviewed the diagnosis, mechanism, and treatment of this disease.PMID:34367414 | PMC:PMC8339718 (Source: International Journal of Clinical and Experimental Pathology)
Source: International Journal of Clinical and Experimental Pathology - August 9, 2021 Category: Pathology Authors: Lin Xia Li Zhang Yue Xiang Liping Liu Zonglin Jing Source Type: research

Intracranial Rosai-Dorfman disease mimicking isolated meningioma: a case report and review of the literature
Int J Clin Exp Pathol. 2021 Jul 15;14(7):827-830. eCollection 2021.ABSTRACTRosai-Dorfman disease is a rare malignant infirmity. Here, we present a case of a 57-year-old man with giddiness and unstable gait, as well as blurred vision in the left eye for four months. Radiologically the diagnosis before surgery was meningioma. The patient received a craniotomy, and the histopathologic diagnosis was Rosai-Dorfman disease. We reviewed the diagnosis, mechanism, and treatment of this disease.PMID:34367414 | PMC:PMC8339718 (Source: International Journal of Clinical and Experimental Pathology)
Source: International Journal of Clinical and Experimental Pathology - August 9, 2021 Category: Pathology Authors: Lin Xia Li Zhang Yue Xiang Liping Liu Zonglin Jing Source Type: research