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Gaucher's disease diagnosed by splenectomy

CONTEXT: Splenectomy continues to find common therapeutic indications for hematologic disorders. In addition, recently it is also performed in surgical clinics to assist diagnose of some illnesses. Gaucher's disease, especially Type I, is the most frequently encountered lysosomal storage disord...

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Autores principales: Adas, Mine, Adas, Gokhan, Karatepe, Oguzhan, Altiok, Merih, Ozcan, Deniz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3364643/
https://www.ncbi.nlm.nih.gov/pubmed/22666685
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author Adas, Mine
Adas, Gokhan
Karatepe, Oguzhan
Altiok, Merih
Ozcan, Deniz
author_facet Adas, Mine
Adas, Gokhan
Karatepe, Oguzhan
Altiok, Merih
Ozcan, Deniz
author_sort Adas, Mine
collection PubMed
description CONTEXT: Splenectomy continues to find common therapeutic indications for hematologic disorders. In addition, recently it is also performed in surgical clinics to assist diagnose of some illnesses. Gaucher's disease, especially Type I, is the most frequently encountered lysosomal storage disorder in man. Manifestations of it are highly variable. The most frequently found symptoms include splenomegaly with anaemia and thrombocytopenia, mostly due to hypersplenism, hepatomegaly and bone disease. CASES: Four patients were reported in the present study. Three of them were easily diagnosed with Gaucher's disease via bone marrow cytology, and one with Gaucher's disease was detected by pathological examination following the splenectomy. CONCLUSIONS: For the pouse of diagnosis of the Gaucher's disease, performing surgery is generally not necessary. However, for the cases of difficult to diagnose by classical methods, the corect diagnosis of Gaucher's disease can only be made by a special operation.
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spelling pubmed-33646432012-06-04 Gaucher's disease diagnosed by splenectomy Adas, Mine Adas, Gokhan Karatepe, Oguzhan Altiok, Merih Ozcan, Deniz N Am J Med Sci Case Report CONTEXT: Splenectomy continues to find common therapeutic indications for hematologic disorders. In addition, recently it is also performed in surgical clinics to assist diagnose of some illnesses. Gaucher's disease, especially Type I, is the most frequently encountered lysosomal storage disorder in man. Manifestations of it are highly variable. The most frequently found symptoms include splenomegaly with anaemia and thrombocytopenia, mostly due to hypersplenism, hepatomegaly and bone disease. CASES: Four patients were reported in the present study. Three of them were easily diagnosed with Gaucher's disease via bone marrow cytology, and one with Gaucher's disease was detected by pathological examination following the splenectomy. CONCLUSIONS: For the pouse of diagnosis of the Gaucher's disease, performing surgery is generally not necessary. However, for the cases of difficult to diagnose by classical methods, the corect diagnosis of Gaucher's disease can only be made by a special operation. Medknow Publications & Media Pvt Ltd 2009-08 /pmc/articles/PMC3364643/ /pubmed/22666685 Text en Copyright: © North American Journal of Medical Sciences http://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
Adas, Mine
Adas, Gokhan
Karatepe, Oguzhan
Altiok, Merih
Ozcan, Deniz
Gaucher's disease diagnosed by splenectomy
title Gaucher's disease diagnosed by splenectomy
title_full Gaucher's disease diagnosed by splenectomy
title_fullStr Gaucher's disease diagnosed by splenectomy
title_full_unstemmed Gaucher's disease diagnosed by splenectomy
title_short Gaucher's disease diagnosed by splenectomy
title_sort gaucher's disease diagnosed by splenectomy
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3364643/
https://www.ncbi.nlm.nih.gov/pubmed/22666685
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