Evidence map›Paper›PMID 42290819›Full record

ArticleClinical case reports2026

Pure Red Cell Aplasia as an Isolated Paraneoplastic Manifestation of Thymoma: A Case Report and Literature Review.

Heba Amer, Modar Alajlani, Mhd Rashad Jamle, Hareth Almanfe, Mohammad Shbat, Mohammad Abd Alrahman Saif, Anas Abdulrazzak, Ahmed Nabhan, Bassam Darwish

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Article in Clinical case reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

9 authors.

Heba AmerDamascus University, Faculty of Medicine Damascus Syrian Arab Republic.ORCID https://orcid.org/0009-0006-6019-2560
Modar AlajlaniDamascus University, Faculty of Medicine Damascus Syrian Arab Republic.ORCID https://orcid.org/0009-0000-4190-9745
Mhd Rashad JamleDamascus University, Faculty of Medicine Damascus Syrian Arab Republic.
Hareth AlmanfeLatakia University, Faculty of Medicine Latakia Syrian Arab Republic.
Mohammad ShbatDepartment of Thoracic Surgery Al Mouwasat Hospital Damascus Syrian Arab Republic.
Mohammad Abd Alrahman SaifDepartment of Thoracic Surgery Al Mouwasat Hospital Damascus Syrian Arab Republic.
Anas AbdulrazzakDepartment of Thoracic Surgery Al Mouwasat Hospital Damascus Syrian Arab Republic.
Ahmed NabhanDepartment of Thoracic Surgery Al Mouwasat Hospital Damascus Syrian Arab Republic.
Bassam DarwishDepartment of Thoracic Surgery Al Mouwasat Hospital Damascus Syrian Arab Republic.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Thymomas are epithelial tumors of the anterior mediastinum and are frequently associated with paraneoplastic autoimmune disorders. Pure red cell aplasia (PRCA) is a rare but clinically significant complication, caused by immune-mediated suppression of erythropoiesis. We report a case of a 52-year-old male with a previously diagnosed but untreated thymoma, who presented after 9 years with severe normocytic, normochromic anemia and reticulocytopenia. Bone marrow examination revealed selective erythroid suppression with preservation of myeloid and megakaryocytic lineages, consistent with PRCA. Imaging demonstrated a large anterior mediastinal mass measuring 16 cm. The patient received supportive blood transfusions followed by surgical thymectomy. Histopathological and immunohistochemical analysis confirmed a mixed spindle cell thymoma (Type A/AB). Postoperatively, the patient achieved complete hematological recovery without additional immunosuppressive therapy. This case highlights that thymoma-associated PRCA may present as an isolated paraneoplastic manifestation without neuromuscular symptoms. It underscores the crucial role of thymectomy in restoring erythropoiesis and achieving transfusion independence. To our knowledge, this is the first reported case of thymoma-associated PRCA in Syria, providing valuable insight for clinicians managing similar rare presentations.

Indexed as

case reportparaneoplastic syndromepure red cell aplasiathymectomythymoma

Identifiers

PMID42290819
PMCPMC13253985

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