Home About us Current issue Ahead of Print Back issues Submission Instructions Advertise Contact Login   

Search Article 
Advanced search 
Saudi Journal of Kidney Diseases and Transplantation
Users online: 871 Home Bookmark this page Print this page Email this page Small font sizeDefault font size Increase font size 

CASE REPORT Table of Contents   
Year : 2009  |  Volume : 20  |  Issue : 6  |  Page : 1076-1078
Epstein syndrome with rapid progression to end stage renal disease

Pediatric Department, King Hussein Medical Center, Amman, Jordan

Click here for correspondence address and email

Date of Web Publication27-Oct-2009


The association of haematological abnormalities and hereditary nephritis is rare; it is mainly included in a spectrum of autosomal dominant macrothrombocytopenias: May-Hegglin anomaly, Fechtner, Sebastian, Epstein and Alport syndrome with macro thrombocytopenia. We are presenting a missed case of a boy who presented with epistaxis and his diagnostic work up revealed macrothrombocytopenia, sensorineural hearing loss and chronic nephropathy which constitute the Epstein syndrome, with rapid deterioration of kidney function.

How to cite this article:
Alhindawi E, Al-Jbour S. Epstein syndrome with rapid progression to end stage renal disease. Saudi J Kidney Dis Transpl 2009;20:1076-8

How to cite this URL:
Alhindawi E, Al-Jbour S. Epstein syndrome with rapid progression to end stage renal disease. Saudi J Kidney Dis Transpl [serial online] 2009 [cited 2023 Feb 4];20:1076-8. Available from: https://www.sjkdt.org/text.asp?2009/20/6/1076/57268

   Introduction Top

Inherited giant platelet disorders represent a group of rare disorders characterised by throm­bocytopenia, giant platelets and variable blee­ding symptoms. [1] All are inherited as autosomal dominant disorders and include:  May-Hegglin anomaly More Details, Sebastian, Fechtner, Epstein, and auto­somal dominant Alport syndrome with platelet defect. [2] Epstein syndrome constitute nephritis with no characteristic features associated with nerve conduction deafness and giant throm­bocytopenia. [3] The syndrome belongs to the MYH9 syndromes and was first described in 1972. [3]

   Case Report Top

A 10 year old boy presented to the hematology clinic with recurrent epistaxis since early child­hood, he was the first child of consanguinous parents, he was known to have mild sensori­neural hearing loss since the age of 5 years, and was first found to have thrombocytopenia after investigating him for jaundice and epis­taxis and at that time his siblings have acute Hepatitis A infection and he was found to have the same infection as them, the full blood count showed a platelet count of 50-80,000 mm, his WBCs and PCV were normal at that time, and a blood film showed giant form platelets, normochromic normocytic RBCs and normal WBCs with no inclusion bodies. A bone marrow aspirate was done and was normal. He was found to have elevated liver enzymes in the ranges of AST 104, ALT 106 and a liver biopsy was done to rule out liver pathology as a cause of these findings, the liver biopsy showed mild inflammatory cells infil-trate with plasma cells and eosinophils and a work up of liver disease excluded metabolic and autoimmune hepatitis.

He was falling below the third centiles for his height and weight on growth charts and for that a bone age assessment was done and was delayed and showed osteoporotic bone changes, at this point the first urine analysis was done for the patient 1 year after starting investiga­ting him and it showed proteinuria, and hema­turia, so was referred to the nephrology clinic for evaluation and there he was found to have blood pressure readings above the 95th centile for his age and height, and his calculated GFR was 65 mL/min/1.73 m, and was considered to have chronic kidney disease and a kidney biopsy was done to diagnose the original pathology, his biopsy findings were consistent with chro­nic kidney disease with sclerosis and fibrosis in the glomeruli as well as focal loss and atro­phy in the tubules [Figure 1].

The patient was screened for hearing and eye abnormalities and his hearing assessment showed bilateral moderate sensorineural hea­ring loss, and his eye examination was normal. With the findings of chronic nephropathy, giant thrombocytopenia, and sensorineural hearing loss the patient was diagnosed to have Epstein syndrome.

Back to the family history in our patient his mother was known to the Obstetric department because of thrombocytopenia and was diagnosed and followed as a case of chronic idiopathic thrombocytopenic purpura and her blood film contained giant platelets as well, she has nor­mal urine analysis and normal kidney function test with no hearing abnormalities. The father and other siblings were all normal, after diag­nosing our patient his mother gave birth to a baby girl who had giant thrombocytopenia and will need follow up for her hearing and kidney function later in life.

To the contrary of what we seen in Alport syndrome our patient showed a rapid deterio­ration in his kidney function over the last year and was started on hemodialysis recently wai­ting for completing the tissue matching and other investigations with his father as a possi­ble live related donor for kidney transplant.

   Discussion Top

The autosomal dominant macrothrombocyto­penias which include: May-Hegglin anomaly, Sebastian, Fechtner, Epstein, and autosomal do­minant Alport with thrombocytopenia are dis­tinguished by different combinations of clini­cal and laboratory signs. [4]

Of the above disorders Epstein syndrome cons­titute macrothrombocytopenia without neutro­phil inclusion bodies in addition to manifes­tations of deafness and nephritis. [5] It is an auto­somal dominant disease and the hearing and renal abnormalities are indistinguishable from those observed in Fechtner syndrome. [6]

It belongs to the MYH9 related hereditary macrothrombocytopenia which include the a­bove mentioned disorders [7] , these pletelets dis­orders are found to be associated with muta­tions in the non muscle myosin heavy chain 9 gene (MYH9) which encode non muscle myo­sin heavy chain IIA (MYHIIA) , [2] and this has been located on the chromosome region22q11­-q13. [8]

This disorder was first described by Epstein et al in 1972 when he described two unrelated families with platelet disorder and mild hea­ring loss as well as renal disease indistingui­shable from that of Alport syndrome. [3] The giant platelets in Epstein syndrome contained granules of normal structure but with an iregular cytoplasm and their survival was normal but the aggregation and excretion in response to collagen, adenosine and thrombin were all decreased, [9] but the results of platelet dysfunc­tion is variable ranging from normal to grossly impaired, [10] and the patient usually present with bleeding tendency which is often mild and can be corrected by donor platelet transfusion. Sple­nectomy does not increase the platelet count, [11] and steroids has no role in the management of thrombocytopenia in this disorder. [10]

In Fechtner syndrome the clinical features include the same findings as in Epstein syn­drome but in addition there is leucocytes in­clusion bodies and eye abnormalities in the form of cataract. [8]

Patients with Epstein syndrome usually pre­sent with renal abnormalities including hema­turia, proteinuria, chronic kidney disease, and hypertension or bleeding tendency, the hearing abnormality is usually mild and discovered du­ring routine screening of patients. [8],[11] The renal abnormalities in Epstein syndrome are variable and has no specific characteristic features with focal segmental glomerulosclerosis being fre­quently reported as well as features of nephro­pathy in Alport syndrome, [8] renal biopsy diag­nosis is mandatory in the absence of family members with same features but in the pre­sence of a diagnosed family member it's not necessary and clinical diagnosis suffices. [11]

We think that our patient is unique for his rapid deterioration of his kidney function since the renal natural history of Epstein syndrome is very similar to Alport syndrome with prog­ression to end stage renal failure in 3rd-4th decade and requirement of renal replacement therapy with both hemodialysis and peritoneal dialysis being suitable modalities of treatment as well as successful renal transplantation. [11]

So in conclusion it's very important to screen patients with macrothrombocytopenia for uri­nary abnormalities since the association is very well known, and we also emphasize the im­portance of a detailed family history in renal problems since hereditary disorders can show different phenotypic features. [11]

   Acknowledgement Top

Special acknowledgement to Dr. Issa Hazza'a for his useful suggestions and continued support.

   References Top

1.Peterson LC, Rao KV, Crosson JK, White JG. Fechtner syndrome: a variant of Alport's syndrome with leukocyte inclusions and macrothrombocytopenia. Blood 1985;65:397-406.  Back to cited text no. 1      
2.Heath KE, Campos_Barros A, Toren A, et al. Non muscle Myosin heavy chain IIA mutation define a specrum of autosomal dominant macrothrombocyto­penia: May-Hegglin Anomaly and Fechtner, Sebastian, Epstein, and Alport like syndromes. Am Hum Genet 2001;69(5):1033-45.  Back to cited text no. 2      
3.Epstein JD, Sahud MA, Piel CF, et al. Hereditary macrothrombocytopenia, nephritis and deafness. Am J Med 1972;52:299-310.  Back to cited text no. 3      
4.Seri M, Pecci A, DiBari F, et al. MYH9-related di­sease: May-Hegglin anomaly, Sebastian syndrome, Fechtner Syndrome, and Epstein syndrome are not distinct entities but represent a variable expression of a single illness. Medicine (Baltimore) 2003;82 (3): 203-15.  Back to cited text no. 4      
5.George JN, Lichtman MA, Coller BS, Kipps TJ. Thrombocytopenia due to diminished or defective platelet production. Hereditary and congenital throm­bocytopenia. Hematology, International edition, New Delhi: McGrow-Hill Inc; 1995:1281-5.  Back to cited text no. 5      
6.Seri M, Savino M, Bordo D, Cusano R: Epstein Syndrome: Another renal disorder with mutations in the non muscle myosin heavy chain 9 genes. Hum Genet 2002;110(2):182-6.  Back to cited text no. 6      
7.Dong F, Li S, Pujol-Moix N, et al. Genotype-pheno­type correlation in MYH9 related thrombocyto­penia. Br J Haematol 2005;130(4):620-7.  Back to cited text no. 7      
8.Prakash S, Chung KW, Sinha S, et al. Autosomal Dominant Prgressive Nephropathy with Deafness: Linkage to a New Locus on Chromosome 11q24. J Am Soc Nephrol 2003;14:1794-803.  Back to cited text no. 8  [PUBMED]  [FULLTEXT]  
9.Berhein J, Dechavanne M, Bryon PA, et al. Throm­bocytopenia, macrothrombocytopathy, nephritis and deafness. Am J Med 1976;61(1):145-50.  Back to cited text no. 9      
10.Quadri M, Ahmad M, Senan K, Al-Sheikh I. Congenital macrothrombocytopenic Thrombopathy and Nephritis (Epstein syndrome - variant). Ann Saudi Med 2000;20:2.  Back to cited text no. 10      
11.Richardson D, Shires M, Davison AM. Renal diag­nosis without renal biopsy, Nephritis and sensori­neural deafness. Nephrol Dial Transplant 2001;16: 1291-4.  Back to cited text no. 11  [PUBMED]  [FULLTEXT]  

Correspondence Address:
Samah Al-Jbour
Pediatric Department, King Hussein Medical Center, P.O. Box 1643, Tariq, Amman
Login to access the Email id

Source of Support: None, Conflict of Interest: None

PMID: 19861875

Rights and PermissionsRights and Permissions


  [Figure 1]

This article has been cited by
1 Cochlear implantation in a patient with Epstein syndrome
Nishiyama, N. and Kawano, A. and Kawaguchi, S. and Shirai, K. and Suzuki, M.
Auris Nasus Larynx. 2013; 40(4): 409-412
2 Plasma from a case of recurrent idiopathic FSGS perturbs non-muscle myosin IIA (MYH9 protein) in human podocytes
Babayeva, S. and Miller, M. and Zilber, Y. and Kares, R.E. and Bernard, C. and Bitzan, M. and Goodyer, P. and Torban, E.
Pediatric Nephrology. 2011; 26(7): 1071-1081
3 Glomerular pathology in autosomal dominant MYH9 spectrum disorders: What are the clues telling us about disease mechanism
Kopp, J.B.
Kidney International. 2010; 78(2): 130-133
4 The May-Hegglin anomaly in a kidney transplant recipient
Fabbian, F. and Ricci, F. and De Giorgi, A. and Forcellini, S. and Scanelli, G.
NDT Plus. 2010; 3(3): 312


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

    Case Report
    Article Figures

 Article Access Statistics
    PDF Downloaded615    
    Comments [Add]    
    Cited by others 4    

Recommend this journal