Evidence map›Paper›PMID 41684973›Full record

ArticleCureus2026

Postpartum-Onset Dermatomyositis Presenting With Malignant Pleural Effusion: A Case Report.

Eesha Zainab, Hamdia Gul Aslam, Ahmad Atif, Muhammad Imran

Abstract readCase Reports
In one paragraph

Article in Cureus, 2026. 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

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0 citing papers in PubMed.

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4 · The record

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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

4 authors.

Eesha ZainabDepartment of Pulmonology, Allama Iqbal Medical College, Lahore, PAK.
Hamdia Gul AslamDepartment of Pulmonology, Allama Iqbal Medical College, Lahore, PAK.
Ahmad AtifDepartment of Pulmonology, Jinnah Hospital, Allama Iqbal Medical College, Lahore, PAK.
Muhammad ImranDepartment of Pathology, Allama Iqbal Medical College, Lahore, PAK.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Dermatomyositis (DM) is a rare autoimmune inflammatory myopathy with cutaneous and muscular manifestations. Malignancy is associated with up to one-third of cases in women; gynecological cancer is among the most frequent associations. Postpartum-onset DM is exceptionally rare, with only a few cases in the literature. We report a case of postpartum-onset DM complicated by malignant pleural effusion. A 40-year-old Pakistani woman, 15 days postpartum following a cesarean section, presented with progressive facial swelling, heliotrope rash, photosensitivity, and proximal muscle weakness. She also reported dysphagia, alopecia, and weight loss. A strong family history of cancer was noted. Electromyography and MRI confirmed an inflammatory myopathy. Subsequently, she developed dyspnea and cough. Imaging revealed a right-sided pleural effusion with pleural nodules. Pleural fluid cytology and biopsy confirmed metastatic adenocarcinoma. Immunohistochemistry was positive for PAX8 and cytokeratin-7, suggesting a gynecological origin, although no primary gynecological tumor was identified on imaging. Positron emission tomography (PET)-computed tomography (CT) and laparoscopic staging were not feasible due to financial and clinical constraints. The patient was started on prednisolone and azathioprine, which significantly improved her DM symptoms. For the malignancy, she began systemic chemotherapy. The pleural effusion was managed with chest tube drainage, pleurodesis, and thoracotomy. Despite treatment, her prognosis remained poor due to advanced metastatic disease. Postpartum-onset DM presenting with malignant pleural effusion is rare and may signal an occult malignancy. This case highlights the importance of early cancer screening in similar presentations, as well as the need for a coordinated, multidisciplinary approach to optimize patient management and outcomes.

Indexed as

case reportdermatomyositismalignant pleural effusionparaneoplastic syndromepostpartum

Identifiers

PMID41684973
PMCPMC12893399

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