An analysis of 30 cases of myelodysplastic syndrome

Myelodysplastic syndrome (MDS) is a clonal disorder of pluripotential stem cells of the bone marrow. The purpose of the study was to obtain epidemiological data of MDS. Thirty cases of MDS presented from April 1998 to May 2006 are included in this study. Complete blood counts were performed in an au...

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Main Authors: Shah Nilam, Prajapati Sanjay, Adesara Rashmin, Patel Ashwin
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2009-04-01
Series:Indian Journal of Pathology and Microbiology
Subjects:
Online Access:http://www.ijpmonline.org/article.asp?issn=0377-4929;year=2009;volume=52;issue=2;spage=206;epage=209;aulast=Shah
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spelling doaj-5c72d44c4be14780b690e3be6111ef882020-11-25T00:02:26ZengWolters Kluwer Medknow PublicationsIndian Journal of Pathology and Microbiology0377-49292009-04-01522206209An analysis of 30 cases of myelodysplastic syndromeShah NilamPrajapati SanjayAdesara RashminPatel AshwinMyelodysplastic syndrome (MDS) is a clonal disorder of pluripotential stem cells of the bone marrow. The purpose of the study was to obtain epidemiological data of MDS. Thirty cases of MDS presented from April 1998 to May 2006 are included in this study. Complete blood counts were performed in an automated cell counter. Bone marrow aspiration, trephine biopsy and chromosomal study were carried out. The dry film was stained using a Romanwasky stain and Perl′s stain. Fifteen cases were male and 15 cases were female. The mean age at presentation was 55 years (range 8-73 years). A majority of the patients presented with weakness (63.33%). Autoimmune manifestations in the form of joint pain were present in 13.33%. Patients were symptomatic for a prolonged period before diagnosis could be reached (average 358.8 days). A majority of the patients had MDS-refractory anemia (MDS-RA) or MDS-RA with excess blasts( MDS-RAEB-2) at presentation. Three patients had chromosomal abnormalities (27.27%). Eight patients (26.7%) were relatively young at presentation, less than 50 years of age. Three (10%) were children. A majority of the patients opted for symptomatic treatment only.http://www.ijpmonline.org/article.asp?issn=0377-4929;year=2009;volume=52;issue=2;spage=206;epage=209;aulast=ShahMyelodysplastic syndromethalidomidecyclosporineciprofloxacinautoimmune
collection DOAJ
language English
format Article
sources DOAJ
author Shah Nilam
Prajapati Sanjay
Adesara Rashmin
Patel Ashwin
spellingShingle Shah Nilam
Prajapati Sanjay
Adesara Rashmin
Patel Ashwin
An analysis of 30 cases of myelodysplastic syndrome
Indian Journal of Pathology and Microbiology
Myelodysplastic syndrome
thalidomide
cyclosporine
ciprofloxacin
autoimmune
author_facet Shah Nilam
Prajapati Sanjay
Adesara Rashmin
Patel Ashwin
author_sort Shah Nilam
title An analysis of 30 cases of myelodysplastic syndrome
title_short An analysis of 30 cases of myelodysplastic syndrome
title_full An analysis of 30 cases of myelodysplastic syndrome
title_fullStr An analysis of 30 cases of myelodysplastic syndrome
title_full_unstemmed An analysis of 30 cases of myelodysplastic syndrome
title_sort analysis of 30 cases of myelodysplastic syndrome
publisher Wolters Kluwer Medknow Publications
series Indian Journal of Pathology and Microbiology
issn 0377-4929
publishDate 2009-04-01
description Myelodysplastic syndrome (MDS) is a clonal disorder of pluripotential stem cells of the bone marrow. The purpose of the study was to obtain epidemiological data of MDS. Thirty cases of MDS presented from April 1998 to May 2006 are included in this study. Complete blood counts were performed in an automated cell counter. Bone marrow aspiration, trephine biopsy and chromosomal study were carried out. The dry film was stained using a Romanwasky stain and Perl′s stain. Fifteen cases were male and 15 cases were female. The mean age at presentation was 55 years (range 8-73 years). A majority of the patients presented with weakness (63.33%). Autoimmune manifestations in the form of joint pain were present in 13.33%. Patients were symptomatic for a prolonged period before diagnosis could be reached (average 358.8 days). A majority of the patients had MDS-refractory anemia (MDS-RA) or MDS-RA with excess blasts( MDS-RAEB-2) at presentation. Three patients had chromosomal abnormalities (27.27%). Eight patients (26.7%) were relatively young at presentation, less than 50 years of age. Three (10%) were children. A majority of the patients opted for symptomatic treatment only.
topic Myelodysplastic syndrome
thalidomide
cyclosporine
ciprofloxacin
autoimmune
url http://www.ijpmonline.org/article.asp?issn=0377-4929;year=2009;volume=52;issue=2;spage=206;epage=209;aulast=Shah
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