An underdiagnosed colonic tumor with a confusing immunophenotype
Ann Pathol. 2023 Oct 24:S0242-6498(23)00197-9. doi: 10.1016/j.annpat.2023.09.003. Online ahead of print.NO ABSTRACTPMID:37884418 | DOI:10.1016/j.annpat.2023.09.003 (Source: Annales de Pathologie)
Source: Annales de Pathologie - October 26, 2023 Category: Pathology Authors: Thomas Coisset Herv é Kinn Bogdan Badic Arnaud Uguen Source Type: research
An underdiagnosed colonic tumor with a confusing immunophenotype
Ann Pathol. 2023 Oct 24:S0242-6498(23)00197-9. doi: 10.1016/j.annpat.2023.09.003. Online ahead of print.NO ABSTRACTPMID:37884418 | DOI:10.1016/j.annpat.2023.09.003 (Source: Annales de Pathologie)
Source: Annales de Pathologie - October 26, 2023 Category: Pathology Authors: Thomas Coisset Herv é Kinn Bogdan Badic Arnaud Uguen Source Type: research
Sea-blue histiocytosis
Ann Pathol. 2023 Oct 19:S0242-6498(23)00202-X. doi: 10.1016/j.annpat.2023.10.001. Online ahead of print.ABSTRACTA 78-year-old woman with hypertrophic cardiomyopathy underwent a septal myomectomy and valve replacement. In the immediate postoperative period she developed shock of mixed etiology and died. At autopsy, hepatomegaly and splenomegaly were identified, with PAS and Giemsa positive intracellular ceroid granular deposits. Sea-blue histiocytosis is an extremely rare, chronic and benign deposit disease. It is characterized by hepatosplenomegaly, thrombocytopenia and lymphadenopathy. The presence of ceroid substance in ...
Source: Annales de Pathologie - October 21, 2023 Category: Pathology Authors: M ónica Bronte Anaut Javier Arredondo Montero Source Type: research
Sea-blue histiocytosis
Ann Pathol. 2023 Oct 19:S0242-6498(23)00202-X. doi: 10.1016/j.annpat.2023.10.001. Online ahead of print.ABSTRACTA 78-year-old woman with hypertrophic cardiomyopathy underwent a septal myomectomy and valve replacement. In the immediate postoperative period she developed shock of mixed etiology and died. At autopsy, hepatomegaly and splenomegaly were identified, with PAS and Giemsa positive intracellular ceroid granular deposits. Sea-blue histiocytosis is an extremely rare, chronic and benign deposit disease. It is characterized by hepatosplenomegaly, thrombocytopenia and lymphadenopathy. The presence of ceroid substance in ...
Source: Annales de Pathologie - October 21, 2023 Category: Pathology Authors: M ónica Bronte Anaut Javier Arredondo Montero Source Type: research
Sea-blue histiocytosis
Ann Pathol. 2023 Oct 19:S0242-6498(23)00202-X. doi: 10.1016/j.annpat.2023.10.001. Online ahead of print.ABSTRACTA 78-year-old woman with hypertrophic cardiomyopathy underwent a septal myomectomy and valve replacement. In the immediate postoperative period she developed shock of mixed etiology and died. At autopsy, hepatomegaly and splenomegaly were identified, with PAS and Giemsa positive intracellular ceroid granular deposits. Sea-blue histiocytosis is an extremely rare, chronic and benign deposit disease. It is characterized by hepatosplenomegaly, thrombocytopenia and lymphadenopathy. The presence of ceroid substance in ...
Source: Annales de Pathologie - October 21, 2023 Category: Pathology Authors: M ónica Bronte Anaut Javier Arredondo Montero Source Type: research
Sea-blue histiocytosis
Ann Pathol. 2023 Oct 19:S0242-6498(23)00202-X. doi: 10.1016/j.annpat.2023.10.001. Online ahead of print.ABSTRACTA 78-year-old woman with hypertrophic cardiomyopathy underwent a septal myomectomy and valve replacement. In the immediate postoperative period she developed shock of mixed etiology and died. At autopsy, hepatomegaly and splenomegaly were identified, with PAS and Giemsa positive intracellular ceroid granular deposits. Sea-blue histiocytosis is an extremely rare, chronic and benign deposit disease. It is characterized by hepatosplenomegaly, thrombocytopenia and lymphadenopathy. The presence of ceroid substance in ...
Source: Annales de Pathologie - October 21, 2023 Category: Pathology Authors: M ónica Bronte Anaut Javier Arredondo Montero Source Type: research
A curious histological pattern of the vas deferens
Ann Pathol. 2023 Oct 13:S0242-6498(23)00201-8. doi: 10.1016/j.annpat.2023.09.007. Online ahead of print.NO ABSTRACTPMID:37839994 | DOI:10.1016/j.annpat.2023.09.007 (Source: Annales de Pathologie)
Source: Annales de Pathologie - October 15, 2023 Category: Pathology Authors: Nicolas Hamadouche Camille Linard C éline Bazille Lionel Vaudreuil Marc Riffet Source Type: research
A curious histological pattern of the vas deferens
Ann Pathol. 2023 Oct 13:S0242-6498(23)00201-8. doi: 10.1016/j.annpat.2023.09.007. Online ahead of print.NO ABSTRACTPMID:37839994 | DOI:10.1016/j.annpat.2023.09.007 (Source: Annales de Pathologie)
Source: Annales de Pathologie - October 15, 2023 Category: Pathology Authors: Nicolas Hamadouche Camille Linard C éline Bazille Lionel Vaudreuil Marc Riffet Source Type: research
A curious histological pattern of the vas deferens
Ann Pathol. 2023 Oct 13:S0242-6498(23)00201-8. doi: 10.1016/j.annpat.2023.09.007. Online ahead of print.NO ABSTRACTPMID:37839994 | DOI:10.1016/j.annpat.2023.09.007 (Source: Annales de Pathologie)
Source: Annales de Pathologie - October 15, 2023 Category: Pathology Authors: Nicolas Hamadouche Camille Linard C éline Bazille Lionel Vaudreuil Marc Riffet Source Type: research
A curious histological pattern of the vas deferens
Ann Pathol. 2023 Oct 13:S0242-6498(23)00201-8. doi: 10.1016/j.annpat.2023.09.007. Online ahead of print.NO ABSTRACTPMID:37839994 | DOI:10.1016/j.annpat.2023.09.007 (Source: Annales de Pathologie)
Source: Annales de Pathologie - October 15, 2023 Category: Pathology Authors: Nicolas Hamadouche Camille Linard C éline Bazille Lionel Vaudreuil Marc Riffet Source Type: research
A curious histological pattern of the vas deferens
Ann Pathol. 2023 Oct 13:S0242-6498(23)00201-8. doi: 10.1016/j.annpat.2023.09.007. Online ahead of print.NO ABSTRACTPMID:37839994 | DOI:10.1016/j.annpat.2023.09.007 (Source: Annales de Pathologie)
Source: Annales de Pathologie - October 15, 2023 Category: Pathology Authors: Nicolas Hamadouche Camille Linard C éline Bazille Lionel Vaudreuil Marc Riffet Source Type: research
A curious histological pattern of the vas deferens
Ann Pathol. 2023 Oct 13:S0242-6498(23)00201-8. doi: 10.1016/j.annpat.2023.09.007. Online ahead of print.NO ABSTRACTPMID:37839994 | DOI:10.1016/j.annpat.2023.09.007 (Source: Annales de Pathologie)
Source: Annales de Pathologie - October 15, 2023 Category: Pathology Authors: Nicolas Hamadouche Camille Linard C éline Bazille Lionel Vaudreuil Marc Riffet Source Type: research
Unusual gluteal localization of unicentric Castleman's disease: A case report and review of the literature
CONCLUSION: The present case is instructive in the work-up of primary soft tissue tumors, for which Castleman's disease is extremely rare and not considered in the differential diagnosis of clinicians. Pathologists must be aware of its existence so that it can be evoked in the presence of a lymphoid population on histological examination.PMID:37798152 | DOI:10.1016/j.annpat.2023.09.005 (Source: Annales de Pathologie)
Source: Annales de Pathologie - October 5, 2023 Category: Pathology Authors: St éphanie Rizzo Alessandra Camboni Pascal Van Eeckhout Patrick Collins Joan Somja Source Type: research
Unusual gluteal localization of unicentric Castleman's disease: A case report and review of the literature
CONCLUSION: The present case is instructive in the work-up of primary soft tissue tumors, for which Castleman's disease is extremely rare and not considered in the differential diagnosis of clinicians. Pathologists must be aware of its existence so that it can be evoked in the presence of a lymphoid population on histological examination.PMID:37798152 | DOI:10.1016/j.annpat.2023.09.005 (Source: Annales de Pathologie)
Source: Annales de Pathologie - October 5, 2023 Category: Pathology Authors: St éphanie Rizzo Alessandra Camboni Pascal Van Eeckhout Patrick Collins Joan Somja Source Type: research
Unusual gluteal localization of unicentric Castleman's disease: A case report and review of the literature
CONCLUSION: The present case is instructive in the work-up of primary soft tissue tumors, for which Castleman's disease is extremely rare and not considered in the differential diagnosis of clinicians. Pathologists must be aware of its existence so that it can be evoked in the presence of a lymphoid population on histological examination.PMID:37798152 | DOI:10.1016/j.annpat.2023.09.005 (Source: Annales de Pathologie)
Source: Annales de Pathologie - October 5, 2023 Category: Pathology Authors: St éphanie Rizzo Alessandra Camboni Pascal Van Eeckhout Patrick Collins Joan Somja Source Type: research
