Evidence map›Paper›PMID 41229648›Full record

ArticleEuropean journal of case reports in internal medicine2025

Disseminated Cryptococcosis: A Diagnostic Challenge in an Immunocompromised Patient.

Paula Mesquita, Daniela Ribeiro Alves, Joana Martinez, Mónica Mata, Ana Micaela Martins, João Fonseca

Abstract read
In one paragraph

Article in European journal of case reports in internal medicine, 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.

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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

6 authors.

Paula MesquitaInternal Medicine Service, Local Health Unit of the Aveiro Region, Aveiro, Portugal.
Daniela Ribeiro AlvesInternal Medicine Service, Local Health Unit of the Aveiro Region, Aveiro, Portugal.
Joana MartinezInfectious Diseases Service, Local Health Unit of the Aveiro Region, Aveiro, Portugal.
Mónica MataInternal Medicine Service, Local Health Unit of the Aveiro Region, Aveiro, Portugal.
Ana Micaela MartinsInfectious Diseases Service, Local Health Unit of the Aveiro Region, Aveiro, Portugal.
João FonsecaInternal Medicine Service, Local Health Unit of the Aveiro Region, Aveiro, Portugal.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Cryptococcosis is an opportunistic fungal infection that causes disseminated disease in immunocompromised patients. Peritoneal involvement is rare and diagnostically challenging. Case report: A 76-year-old man with Crohn's disease on infliximab and previously treated latent tuberculosis was admitted with constitutional symptoms and abdominal distention evolving over 5 months. Ultrasound revealed bilateral pleural effusion and ascites. Initial hypotheses-peritoneal carcinomatosis and tuberculosis-were excluded through computed tomography scan, laboratory tests, and exploratory laparoscopy with biopsy, which showed necrotizing granulomatous peritonitis. Disseminated cryptococcosis was confirmed by India ink staining, cultures from peritoneal and pleural fluids, and serum cryptococcal antigen. Cerebrospinal fluid analysis and ophthalmological evaluation excluded central nervous system and ocular involvement. Treatment with liposomal amphotericin B and flucytosine led to clinical improvement. Conclusion: This case highlights the importance of considering cryptococcosis in the differential diagnosis of polyserositis in immunocompromised patients. Early diagnosis and antifungal therapy improve outcomes. LEARNING POINTS: Disseminated cryptococcosis, although rare, should be considered in the differential diagnosis of polyserositis and necrotizing granulomatous peritonitis in immunocompromised patients.Cryptococcus can closely mimic tuberculosis or peritoneal carcinomatosis; negative mycobacterial studies should prompt fungal investigations, including cryptococcal antigen testing.Early diagnosis and timely initiation of antifungal therapy are crucial to reduce morbidity and mortality, with treatment tailored to comorbidities such as renal dysfunction.

Indexed as

constitutional syndromeCrohn’s diseaseDisseminated cryptococcosisimmunocompromised patientnecrotizing granulomas

Identifiers

PMID41229648
PMCPMC12604883

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