Therapeutic plasma exchange in gastric signet ring cell carcinoma presenting as microangiopathic hemolytic anemia: A rare case report.


Journal

Journal of clinical apheresis
ISSN: 1098-1101
Titre abrégé: J Clin Apher
Pays: United States
ID NLM: 8216305

Informations de publication

Date de publication:
Dec 2022
Historique:
revised: 12 08 2022
received: 02 06 2022
accepted: 29 08 2022
pubmed: 21 9 2022
medline: 3 12 2022
entrez: 20 9 2022
Statut: ppublish

Résumé

Microangiopathic hemolytic anemia (MAHA) defines a group of disorders characterized by the formation of microthrombi in capillaries and arterioles and the fragmentation of erythrocytes that pass through. Cancer-related MAHA is a rare but serious condition that is encountered in patients diagnosed with a malignancy. This clinical picture is thought to be linked to certain tumor characteristics; particularly, adenocarcinoma histology, vascular invasion, and bone marrow infiltration. MAHA is most commonly associated with tumors of gastric, prostate, and breast origin. The optimal treatment is not clear; however, there is evidence for the importance of promptly starting an effective antineoplastic regimen and it was also reported that administering therapeutic plasma exchange (TPE) therapy for immunocomplex removal could be beneficial for patients with symptoms of bleeding and thrombosis. Here, we present a case that presented a picture of MAHA secondary to gastric signet-ring cell adenocarcinoma (SRCC). The clinical picture was initially evaluated as thrombotic thrombocytopenic purpura and the patient benefited significantly from the TPE treatment administered before the adenocarcinoma diagnosis was confirmed. In this period, epistaxis stopped, platelet count increased from 25 × 10

Identifiants

pubmed: 36125111
doi: 10.1002/jca.22013
doi:

Types de publication

Case Reports

Langues

eng

Sous-ensembles de citation

IM

Pagination

606-610

Informations de copyright

© 2022 Wiley Periodicals LLC.

Références

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Auteurs

Omer Candar (O)

Department of Hematology, Faculty of Medicine, Uludag University, Bursa, Turkey.

Omer Ekinci (O)

Department of Hematology, Faculty of Medicine, Fırat University, Elazığ, Turkey.

Mustafa Merter (M)

Department of Hematology, Faculty of Medicine, Fırat University, Elazığ, Turkey.

Mehmet Aslan (M)

Department of Hematology, Faculty of Medicine, Fırat University, Elazığ, Turkey.

Ibrahim Aras (I)

Department of Pathology, Faculty of Medicine, Yüzüncü Yıl University, Van, Turkey.

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