The Etiology and Diagnosis of Primary Myelofibrosis: Case Study

Indu, M. B. and Khan, Saima and Sharma, Brijesh and Jyotsana, P. Lalita (2022) The Etiology and Diagnosis of Primary Myelofibrosis: Case Study. Asian Journal of Case Reports in Medicine and Health, 7 (2). pp. 11-15.

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Abstract

Primary myelofibrosis is a myeloproliferative neoplasm. It is the rarest among the group of myeloproliferative neoplasms and the incidence is 0.1-1 per 1,00,000 per year. This is characterised by the replacement of normal marrow by fibrous tissue. Patients may present with hepatosplenomegaly due to extramedullary erythropoiesis. A high index of suspicion is needed to diagnose the same. This study describes a case that was diagnosed to have myelofibrosis when he presented with splenomegaly as a main symptom.

Item Type: Article
Subjects: Opene Prints > Medical Science
Depositing User: Managing Editor
Date Deposited: 21 Feb 2023 06:49
Last Modified: 17 May 2024 09:40
URI: http://geographical.go2journals.com/id/eprint/1419

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