Evidence map›Paper›PMID 40597173›Full record

ArticleJournal of medical case reports2025

Essential thrombocythemia as an initial presentation of polyneuropathy, organomegaly, endocrinopathy, M-protein, skin changes syndrome with complete response to the bortezomib, cyclophosphamide, dexamethasone regimen: a case report.

Alireza Zangooie, Zahra Moradi, Reza Asgari, Amirhosein Maharati, Zahra Salehi, Abolghasem Allahyari

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Article in Journal of medical case reports, 2025. 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

6 authors.

Alireza ZangooieStudent Research Committee, Birjand University of Medical Sciences, Birjand, Iran.
Zahra MoradiSchool of Medicine, Tehran University of Medical Sciences, Tehran, Iran.
Reza AsgariStudent Research Committee, Qazvin University of Medical Sciences, Qazvin, Iran.
Amirhosein MaharatiStudent Research Committee, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.
Zahra SalehiHematology, Oncology and Stem Cell Transplantation Research Center, Research Institute for Oncology, Hematology and Cell Therapy, Tehran University of Medical Sciences, Tehran, Iran. zahra.salehi6463@yahoo.com.
Abolghasem AllahyariDivision of Hematology and Oncology, Department of Internal Medicine, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran. allahyaria@mums.ac.ir.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPolyneuropathy, organomegaly, endocrinopathy, M-protein, skin changes syndrome is a rare paraneoplastic disorder often presenting with atypical manifestations, making diagnosis challenging. This case is novel due to the rare presentation of essential thrombocythemia as the initial manifestation of polyneuropathy, organomegaly, endocrinopathy, M-protein, skin changes syndrome. Furthermore, it highlights the remarkable therapeutic response, achieving a complete remission following treatment with the bortezomib, cyclophosphamide, dexamethasone regimen, underscoring this combination therapy's efficacy in managing such complex cases. CASE PRESENTATION: A 65-year-old Iranian woman presented with fatigue, headache, and thrombocytosis, leading to a diagnosis of essential thrombocythemia. Over time, her condition progressed with the development of neuropathy and persistence of thrombocytosis, which warranted further investigation. Imaging revealed multiple lymphadenopathies, sclerotic bone lesions, and ascitic fluid, raising suspicion for a plasma cell dyscrasia. Bone marrow biopsy, lymph node biopsy, and elevated vascular endothelial growth factor levels confirmed the diagnosis of polyneuropathy, organomegaly, endocrinopathy, M-protein, skin changes syndrome. The patient was treated with bortezomib, cyclophosphamide, dexamethasone chemotherapy regimen, resulting in complete symptom relief, normalization of the complete blood count, and significant improvement in imaging findings.

conclusionThis case highlights the need to recognize atypical polyneuropathy, organomegaly, endocrinopathy, M-protein, skin changes syndrome presentations, such as essential thrombocythemia, for timely diagnosis and underscores the bortezomib, cyclophosphamide, dexamethasone regimen's efficacy in achieving complete remission.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsThrombocythemia, EssentialAgedBortezomibCyclophosphamideDexamethasoneFemaleHumansPOEMS SyndromeTreatment OutcomeBortezomibCyclophosphamideDexamethasoneCase reportComplete responseEssential thrombocythemiaInitial presentationPOEMS syndromeVCD regimen

Identifiers

PMID40597173
PMCPMC12220048

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