Challenges in Diagnosing Polycythemia Vera in Primary Care: A 55-Year-Old Malaysian Woman with Atypical Presentation

Objective: Mistake in diagnosis Background: Polycythemia vera (PV) is a myeloproliferative neoplasm (MPNs) marked by elevated hemoglobin and hemato-crit, which can lead to thromboembolic events and progress to myelofibrosis or acute myeloid leukemia (AML). MPNs, including PV, are relatively rare in...

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Published in:American Journal of Case Reports
Main Author: Paiman N.S.H.; Nasir N.M.; Miptah H.N.; Saidon N.; Monir M.A.
Format: Article
Language:English
Published: International Scientific Information, Inc. 2024
Online Access:https://www.scopus.com/inward/record.uri?eid=2-s2.0-85204041566&doi=10.12659%2fAJCR.944202&partnerID=40&md5=b03a1915c50f4c53486a1dc81c7b4575
id 2-s2.0-85204041566
spelling 2-s2.0-85204041566
Paiman N.S.H.; Nasir N.M.; Miptah H.N.; Saidon N.; Monir M.A.
Challenges in Diagnosing Polycythemia Vera in Primary Care: A 55-Year-Old Malaysian Woman with Atypical Presentation
2024
American Journal of Case Reports
25

10.12659/AJCR.944202
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85204041566&doi=10.12659%2fAJCR.944202&partnerID=40&md5=b03a1915c50f4c53486a1dc81c7b4575
Objective: Mistake in diagnosis Background: Polycythemia vera (PV) is a myeloproliferative neoplasm (MPNs) marked by elevated hemoglobin and hemato-crit, which can lead to thromboembolic events and progress to myelofibrosis or acute myeloid leukemia (AML). MPNs, including PV, are relatively rare in Malaysia, and there is currently no recent published data reporting the demographics and outcomes of PV patients in the country. In Western countries, routine annual blood tests are standard, whereas this practice is less common in Malaysia, underscoring the need for improved awareness and accessibility to ensure timely diagnosis of PV. Case Report: This report presents a case of a 55-year-old Malaysian woman in a primary care setting, initially misdiagnosed with benign conditions due to atypical presentations of recurrent bilateral eye redness and dizziness. Persistent symptoms led to further evaluation by primary care and hematologist, which revealed elevated hemoglobin, hematocrit, leukocytosis, JAK2 V617F mutation, and low serum erythropoietin levels, confirming PV, even with-out proceeding with a bone marrow biopsy. Treatment with phlebotomy, hydroxyurea, and aspirin resulted in significant improvements in ocular symptoms and hematological parameters within 60 days. Conclusions: This case underscores the critical role of primary care in the early detection of polycythemia vera. Timely identification and appropriate referral from primary care settings are essential to avoid diagnostic delays and ensure effective management, improving patient outcomes and preventing complications. © Am J Case Rep, 2024.
International Scientific Information, Inc.
19415923
English
Article
All Open Access; Hybrid Gold Open Access
author Paiman N.S.H.; Nasir N.M.; Miptah H.N.; Saidon N.; Monir M.A.
spellingShingle Paiman N.S.H.; Nasir N.M.; Miptah H.N.; Saidon N.; Monir M.A.
Challenges in Diagnosing Polycythemia Vera in Primary Care: A 55-Year-Old Malaysian Woman with Atypical Presentation
author_facet Paiman N.S.H.; Nasir N.M.; Miptah H.N.; Saidon N.; Monir M.A.
author_sort Paiman N.S.H.; Nasir N.M.; Miptah H.N.; Saidon N.; Monir M.A.
title Challenges in Diagnosing Polycythemia Vera in Primary Care: A 55-Year-Old Malaysian Woman with Atypical Presentation
title_short Challenges in Diagnosing Polycythemia Vera in Primary Care: A 55-Year-Old Malaysian Woman with Atypical Presentation
title_full Challenges in Diagnosing Polycythemia Vera in Primary Care: A 55-Year-Old Malaysian Woman with Atypical Presentation
title_fullStr Challenges in Diagnosing Polycythemia Vera in Primary Care: A 55-Year-Old Malaysian Woman with Atypical Presentation
title_full_unstemmed Challenges in Diagnosing Polycythemia Vera in Primary Care: A 55-Year-Old Malaysian Woman with Atypical Presentation
title_sort Challenges in Diagnosing Polycythemia Vera in Primary Care: A 55-Year-Old Malaysian Woman with Atypical Presentation
publishDate 2024
container_title American Journal of Case Reports
container_volume 25
container_issue
doi_str_mv 10.12659/AJCR.944202
url https://www.scopus.com/inward/record.uri?eid=2-s2.0-85204041566&doi=10.12659%2fAJCR.944202&partnerID=40&md5=b03a1915c50f4c53486a1dc81c7b4575
description Objective: Mistake in diagnosis Background: Polycythemia vera (PV) is a myeloproliferative neoplasm (MPNs) marked by elevated hemoglobin and hemato-crit, which can lead to thromboembolic events and progress to myelofibrosis or acute myeloid leukemia (AML). MPNs, including PV, are relatively rare in Malaysia, and there is currently no recent published data reporting the demographics and outcomes of PV patients in the country. In Western countries, routine annual blood tests are standard, whereas this practice is less common in Malaysia, underscoring the need for improved awareness and accessibility to ensure timely diagnosis of PV. Case Report: This report presents a case of a 55-year-old Malaysian woman in a primary care setting, initially misdiagnosed with benign conditions due to atypical presentations of recurrent bilateral eye redness and dizziness. Persistent symptoms led to further evaluation by primary care and hematologist, which revealed elevated hemoglobin, hematocrit, leukocytosis, JAK2 V617F mutation, and low serum erythropoietin levels, confirming PV, even with-out proceeding with a bone marrow biopsy. Treatment with phlebotomy, hydroxyurea, and aspirin resulted in significant improvements in ocular symptoms and hematological parameters within 60 days. Conclusions: This case underscores the critical role of primary care in the early detection of polycythemia vera. Timely identification and appropriate referral from primary care settings are essential to avoid diagnostic delays and ensure effective management, improving patient outcomes and preventing complications. © Am J Case Rep, 2024.
publisher International Scientific Information, Inc.
issn 19415923
language English
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accesstype All Open Access; Hybrid Gold Open Access
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