Evidence map›Paper›PMID 40893811›Full record

ArticleJournal of medicine and life2025

Splenic marginal zone lymphoma associated with chronic inflammatory demyelinating polyradiculoneuropathy: a case report.

Tarek Mohammed, Halimah Saleh, Huda Albraim, Sariya Khan, Sahar Albraim, Deema Bakhashab

Abstract readCase Reports
In one paragraph

Article in Journal of medicine and life, 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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0citing papers in PubMed
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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Tarek MohammedDepartment of Hematology, Saudi German Hospital, Jeddah, Saudi Arabia.
Halimah SalehDepartment of Internal Medicine, Saudi German Hospital, Jeddah, Saudi Arabia.
Huda AlbraimGeneral Practice, My Clinic, Jeddah, Saudi Arabia.
Sariya KhanGeneral Medicine Practice Program, Batterjee Medical College, Jeddah, Saudi Arabia.
Sahar AlbraimGeneral Practice, My Clinic, Jeddah, Saudi Arabia.
Deema BakhashabDepartment of Internal Medicine, Soliman Fakeeh Hospital, Jeddah, Saudi Arabia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chronic inflammatory demyelinating polyradiculopathy (CIDP) is an acquired immune-mediated neuropathy characterized by progressive or relapsing-remitting proximal and distal weakness. Lymphomas are among various hematological malignancies associated with CIDP. Splenic marginal zone lymphoma (SMZL) is a rare, indolent B-cell non-Hodgkin lymphoma that classically presents with splenomegaly and cytopenia. The co-occurrence of SMZL and CIDP is extremely rare; the diagnosis thus presents a unique challenge both diagnostically and therapeutically. We report a 65-year-old male patient with progressive proximal weakness, night sweats, and splenomegaly. Investigations revealed pancytopenia with imaging studies confirming the splenomegaly. Further investigations, such as a bone marrow biopsy and histopathology of the spleen, were indicative of a hypocellular marrow and SMZL, respectively. Simultaneously, a diagnosis of CIDP was established based on clinical findings, as well as electromyography and nerve conduction studies. For CIDP, immunosuppressive therapy was initiated; however, no treatment was administered for SMZL due to its indolent nature. He showed partial neurological improvement with the treatment given for CIDP. This underlines the importance of treating both diseases. The rare association of CIDP and SMZL is presented in this case, highlighting the importance of a comprehensive diagnostic workup in patients with neurological and hematological abnormalities. Therefore, for the management of such patients, timely identification and appropriate therapeutic approaches will be necessary for an improved outcome.

Indexed as

Lymphoma, B-Cell, Marginal ZonePolyradiculoneuropathy, Chronic Inflammatory DemyelinatingSplenic NeoplasmsAgedHumansMalecase reportchronic inflammatory demyelinating polyradiculoneuropathyCIDPSMZLsplenic marginal zone lymphoma

Identifiers

PMID40893811
PMCPMC12393300

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.