Home | About us | Editorial board | Search | Ahead of print | Current issue | Archives | Submit article | Instructions | Subscribe | Contacts | Advertise | Login 
 
Search Article 
  
Advanced search 
  Users Online: 41 Home Print this page Email this page Small font sizeDefault font sizeIncrease font size  

 
Table of Contents
LETTER TO THE EDITOR
Year : 2013  |  Volume : 17  |  Issue : 4  |  Page : 767-768

Gaucher disease in a 53-year-old Iranian man


Department of Hematology/Medical Oncology,Urmia University of Medical Sciences, Resident, Department of Internal Medicine, Urmia University of Medical Sciences, Urmia, Iran

Date of Web Publication20-Jun-2013

Correspondence Address:
Nasim Valizadeh
Department of Hematology/Medical Oncology, Urmia University of Medical Sciences, Urmia
Iran
Login to access the Email id

Source of Support: None, Conflict of Interest: None


DOI: 10.4103/2230-8210.113782

Rights and Permissions

How to cite this article:
Valizadeh N, Vossoghian S. Gaucher disease in a 53-year-old Iranian man. Indian J Endocr Metab 2013;17:767-8

How to cite this URL:
Valizadeh N, Vossoghian S. Gaucher disease in a 53-year-old Iranian man. Indian J Endocr Metab [serial online] 2013 [cited 2020 Feb 18];17:767-8. Available from: http://www.ijem.in/text.asp?2013/17/4/767/113782

Sir,

Gaucher disease (GD) is a rare genetic disorder. Glucocerebrosidase deficiency affects metabolism of cellular glycolipids, thus glucocerebroside deposites in the lysosomes of cells. GD is more common in the Ashkenazi Jewish population. [1]

Non-neuronopathic form (type-1, GD1) includes more than 90% of cases. [2] Acute neuronopathic form (type-2, GD2) includes 1% of cases and causes to death during infancy or the 1 st years of life. [3]

Subacute or chronic neuronopathic form (GD3) includes 5% of cases and has a slower and later onset than GD2 and leads to death during childhood or early adulthood. [3]

A 53-year-old man was admitted with pancytopenia. He had history of easy bruising and prolonged bleeding following dental extraction for a long period. He had no fever, night sweat, and weight loss. Physical examination revealed massive hepatosplenomegaly. Laboratory findings were included: WBC = 2,800/μl, Hb = 8.5 g/dl, and PLT = 15,000/μl. Erythrocyte sedimentation rate (ESR), renal and liver function tests were normal. Abdominal sonography showed a huge nodular splenomegaly. Bone marrow aspiration showed a hypercellular polymorph marrow with increased megakaryopoiesis and an increased in number of macrophages with a crumpled tissue paper appearance and displaced nuclei (Gaucher cells) [Figure 1]. Bone marrow biopsy showed sheets of Gaucher cells [Figure 2]. The diagnosis of GD was made. Patient's blood sample was sent to Austria for enzyme assay.
Figure 1: A large macrophage with a crumpled tissue paper appearance and displaced nuclei (×1000)

Click here to view
Figure 2: Bone marrow biopsy, sheets of the Gaucher cells (×1000)

Click here to view


GD1 has asymptomatic or symptomatic variants. Symptomatic form present during childhood or the late adulthood but seldom may present in elderly. [4],[5]

In this 53-year-old Iranian Muslim with GD1, all of his six siblings were asymptomatic in ages between 60 years and 80 years. Although he had prolonged bleeding and easy bruising for a long period, he did not take any medical attention. GD1 can occur in higher ages without positive family history. We should consider GD1 in differential diagnosis of pancytopenia and organomegaly in old age patients even in the absence of positive family history for GD.


   Acknowledgment Top


We express our appreciation to Drs. Abbas Saffarifard and Aida Gheibi, residents of the Pathology Department in Urmia University of Medical Sciences who helped us in taking photo from pathology slides of this patient.

 
   References Top

1.Meikle PJ, Hopwood JJ, Clague AE, Carey WF. Prevalence of lysosomal storage disorders. JAMA 1999;281:249-54.  Back to cited text no. 1
    
2.Koprivica V, Stone DL, Park JK, Callahan M, Frisch A, Cohen IJ, et al. Analysis and classification of 304 mutant alleles in patients with type 1 and type 3 Gaucher disease. Am J Hum Genet 2000;66:1777-86.  Back to cited text no. 2
    
3.Gaucher disease: Pathogenesis, clinical manifestations, and diagnosis. Up to Date 20.2.  Back to cited text no. 3
    
4.Elshimali Y, Ganjian S. Gaucher's disease in a 72-year-old man: Case report and review of literature. Internet J Pathol 2007;6.  Back to cited text no. 4
    
5.Mankin HJ, Trahan CA, Barnett NA, Laughead J, Bove CM, Pastores GM. A questionnaire study for 128 patients with Gaucher disease. Clin Genet 2006;69:209-17.  Back to cited text no. 5
    


    Figures

  [Figure 1], [Figure 2]



 

Top
 
  Search
 
    Similar in PUBMED
   Search Pubmed for
   Search in Google Scholar for
    Access Statistics
    Email Alert *
    Add to My List *
* Registration required (free)  

 
  In this article
   Acknowledgment
    References
    Article Figures

 Article Access Statistics
    Viewed910    
    Printed10    
    Emailed0    
    PDF Downloaded183    
    Comments [Add]    

Recommend this journal