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Case report on unusual tumor with synchronous cutaneous and gastrointestinal tract involvement

Histiocytic sarcoma (HS) is an exceedingly rare lymphohematopoietic malignancy with morphological and immunophenotypic characteristics of mature tissue histiocytes. We report a unique case of a HS with synchronous skin and gastrointestinal tract involvement which has not been reported in literature...

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Autores principales: Raj, Aditi, Gaikwad, Vaishali, Amarapurkar, Anjali
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Qassim Uninversity 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8220644/
https://www.ncbi.nlm.nih.gov/pubmed/34234635
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author Raj, Aditi
Gaikwad, Vaishali
Amarapurkar, Anjali
author_facet Raj, Aditi
Gaikwad, Vaishali
Amarapurkar, Anjali
author_sort Raj, Aditi
collection PubMed
description Histiocytic sarcoma (HS) is an exceedingly rare lymphohematopoietic malignancy with morphological and immunophenotypic characteristics of mature tissue histiocytes. We report a unique case of a HS with synchronous skin and gastrointestinal tract involvement which has not been reported in literature till date to the best of our knowledge. A 70-year-old male farmer presented with multiple ulcerated skin lesions ranging from 0.5 to 10 cm all over the body. Autopsy revealed multiple transmural nodular deposits in stomach, intestines, head of pancreas, and peripancreatic tissue. Histopathology and immunohistochemistry profile was consistent with HS exhibiting positivity for CD68, CD163, and lysozyme. CD 163 identifies histiocytic malignancies with high degree of specificity and has become a promising marker for their diagnosis.
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spelling pubmed-82206442021-07-06 Case report on unusual tumor with synchronous cutaneous and gastrointestinal tract involvement Raj, Aditi Gaikwad, Vaishali Amarapurkar, Anjali Int J Health Sci (Qassim) Case Report Histiocytic sarcoma (HS) is an exceedingly rare lymphohematopoietic malignancy with morphological and immunophenotypic characteristics of mature tissue histiocytes. We report a unique case of a HS with synchronous skin and gastrointestinal tract involvement which has not been reported in literature till date to the best of our knowledge. A 70-year-old male farmer presented with multiple ulcerated skin lesions ranging from 0.5 to 10 cm all over the body. Autopsy revealed multiple transmural nodular deposits in stomach, intestines, head of pancreas, and peripancreatic tissue. Histopathology and immunohistochemistry profile was consistent with HS exhibiting positivity for CD68, CD163, and lysozyme. CD 163 identifies histiocytic malignancies with high degree of specificity and has become a promising marker for their diagnosis. Qassim Uninversity 2021 /pmc/articles/PMC8220644/ /pubmed/34234635 Text en Copyright: © International Journal of Health Sciences https://creativecommons.org/licenses/by-nc-sa/3.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Raj, Aditi
Gaikwad, Vaishali
Amarapurkar, Anjali
Case report on unusual tumor with synchronous cutaneous and gastrointestinal tract involvement
title Case report on unusual tumor with synchronous cutaneous and gastrointestinal tract involvement
title_full Case report on unusual tumor with synchronous cutaneous and gastrointestinal tract involvement
title_fullStr Case report on unusual tumor with synchronous cutaneous and gastrointestinal tract involvement
title_full_unstemmed Case report on unusual tumor with synchronous cutaneous and gastrointestinal tract involvement
title_short Case report on unusual tumor with synchronous cutaneous and gastrointestinal tract involvement
title_sort case report on unusual tumor with synchronous cutaneous and gastrointestinal tract involvement
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8220644/
https://www.ncbi.nlm.nih.gov/pubmed/34234635
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