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Primary intracranial leiomyoma in an immunocompetent patient.

Primary intracranial leiomyoma in an immunocompetent patient. Clin Neuropathol. 2018 Jan 10;: Authors: Alvarez R, Schild M, Cummings TJ PMID: 29319490 [PubMed - as supplied by publisher]
Source: Clinical Neuropathology - Category: Pathology Authors: Tags: Clin Neuropathol Source Type: research

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In conclusion, we confirmed the high frequency of the MED12 mutation in uterine leiomyomas of South Korean patients. We also identified various MED12 mutation status in patients with multiple leiomyomas. This suggests that in a given patient, different tumors may have arisen from different cell origins and therefore it is supposed that occurrence of multiple leiomyoma in a single patient may not be caused by intrauterine metastasis or dissemination. PMID: 29333096 [PubMed - in process]
Source: International Journal of Medical Sciences - Category: Biomedical Science Tags: Int J Med Sci Source Type: research
ConclusionsThe etiological diagnosis of acute intestinal obstruction during pregnancy is not easy, especially in the context of a low-income country where the means of biological and radiological diagnosis are lacking. A laparotomy is required before diagnosis of acute surgical abdomen and its management will depend on the intraoperative findings and the condition of the patient.
Source: Journal of Medical Case Reports - Category: General Medicine Source Type: research
In this study, we report the case of a 27-year-old misdiagnosed carrier of HLRCC phenotype, who presented with a large solitary Type II papillary RCC.
Source: Urology Annals - Category: Urology & Nephrology Authors: Source Type: research
This article is protected by copyright. All rights reserved.
Source: Digestive Endoscopy - Category: Gastroenterology Authors: Tags: DEN Video Article Source Type: research
Conclusion The echogenicity of granular cell tumors was similar to that of the submucosal layer, and it was significantly higher than that of leiomyomas. Endoscopic ultrasonography images facilitate the accurate identification of esophageal granular cell tumors. PMID: 29321437 [PubMed - as supplied by publisher]
Source: Internal Medicine - Category: Internal Medicine Tags: Intern Med Source Type: research
AbstractHereditary leiomyomatosis and renal cell carcinoma (HLRCC) syndrome is a rare autosomal dominant disease caused by germline mutations in the fumarate hydratase (FH) gene. Affected individuals develop cutaneous and uterine leiomyomas and aggressive RCC. To date, only few publications described the frequency and morphology of FH-deficient uterine leiomyomas. We reviewed 22 cases collected over 8  years from routine and consultation files based on distinctive histological features. In addition, we screened 580 consecutive uterine leiomyomas from 484 patients, 23 extra-uterine and 8 uterine leiomyosarcomas, and 6 ...
Source: Virchows Archiv - Category: Pathology Source Type: research
Source: American Journal of Obstetrics and Gynecology - Category: OBGYN Authors: Tags: Images in Gynecology Source Type: research
Conclusions PRPL is a rare extrauterine entity probably derived from remnant embryogenic cells. The absence of clinical guidelines recommend an individualized treatment of these patients. Karakousis’s abdominoinguinal approach should be present in any surgeon's armamentarium as the resectability-rate of tumors of the lower quadrant of the abdomen increases up to 95%.
Source: International Journal of Surgery Case Reports - Category: Surgery Source Type: research
va Raja
Source: The American Journal of Gastroenterology - Category: Gastroenterology Authors: Source Type: research
Black women with central centrifugal cicatricial alopecia (CCCA) are at increased risk for developing uterine leiomyomas (ULs), according to a retrospective study.Reuters Health Information
Source: Medscape Pathology Headlines - Category: Pathology Tags: Pathology & Lab Medicine News Source Type: news
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