Pure Red Cell Aplasia Associated with Thymolipoma: Complete Anaemia Resolution following Thymectomy

Author:

Ferreira David12ORCID,Ponraj Royston2,Yeung Adrian3,de Malmanche Jillian4

Affiliation:

1. Conjoint Associate Lecturer, University of New South Wales, Sydney, Australia

2. Medical Department, Medical Registrar, Liverpool Hospital, Elizabeth St., Liverpool, NSW 2170, Australia

3. Haematology Department, Haematology Advanced Trainee, Liverpool Hospital, Elizabeth St., Liverpool, NSW 2170, Australia

4. Haematology Department, Haematology Staff Specialist, John Hunter Hospital, Lookout Rd., New Lambton Heights, NSW 2305, Australia

Abstract

Pure red cell aplasia is an uncommon cause of anaemia rarely associated with thymoma. A combination of immunosuppressive therapy and thymectomy offers a potential cure. Thymectomy alone rarely results in anaemia resolution. A seventy-three-year-old male with Klinefelter syndrome presented with progressively increasing shortness of breath and anaemia. Serological testing supported primary bone marrow pathology, and a bone marrow biopsy was performed. A pure red cell aplasia was seen on bone marrow examination, and computed tomography of the chest demonstrated a thymoma. Thymectomy was performed, and histology revealed a thymolipoma. Complete anaemia resolution was achieved following thymectomy alone. This suggests that thymomas may directly mediate immune dysregulation resulting in erythroid precursor destruction.

Publisher

Hindawi Limited

Subject

Cell Biology,Developmental Biology,Embryology,Anatomy

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