S5157 Coccidioidal Peritonitis: A Rare Manifestation of Disseminated Coccidioidomycosis

Introduction: Disseminated coccidioidomycosis, primarily a pulmonary process, can rarely extend to extrapulmonary sites with significant morbidity. Peritoneal involvement is atypical and may mimic peritoneal carcinomatosis. In endemic regions, coccidioidal peritonitis should be in the differential of patients presenting with vague abdominal symptoms, weight loss, and imaging with omental caking and ascites. Risk factors include immunocompromise and living in regions of dry climates with dusty conditions. Comprehensive evaluation can necessitate imaging, serology, and histopathology. Case Description/Methods: A 55-year-old man from Southern California’s desert valley region presented with several months progressive abdominal discomfort and unintentional weight loss. Computed tomography (CT) imaging of the chest revealed a spiculated pulmonary nodule with mediastinal lymphadenopathy; abdominal CT revealed a diffusely thickened peritoneum, ascites, and omental caking. Diagnostic paracentesis revealed high protein and low serum-ascites albumin gradient concerning for peritoneal carcinomatosis. Given the patient's geographical history and imaging findings serologic testing for Coccidioides was ordered, revealing elevated IgM and IgG titers. Coccidioides complement fixation testing was also positive with a titer of 1:512, supportive of a diagnosis of disseminated coccidioidomycosis. A subsequent biopsy of an infected neck epidermal cyst revealed granulomatous inflammation with large spherules containing endospores consistent with coccidioidomycosis, further supporting the diagnosis. High-dose fluconazole (800 mg daily) led to symptomatic and radiographic improvement. Discussion: While disseminated coccidioidomycosis represents 5-10% of cases, peritoneal involvement is rare as gastrointestinal dissemination occurs in only 2.4%. In this immunocompetent patient from a Coccidiomycosis endemic region, though the initial imaging findings suggested malignancy, a high index of suspicion for this infection led to his appropriate work up and eventual diagnosis. High-dose fluconazole therapy (800 mg daily) has been reported to be effective in disseminated disease. Early recognition and treatment is important to minimize morbidity and mortality. This case of coccidiodal peritonitis highlights the need for awareness to include fungal infections in the differential for patients living in endemic areas where coccidioidomycosis can masquerade as malignancy.

Publication Details

Journal
The American Journal of Gastroenterology
Published
2025-10-01
DOI
https://doi.org/10.14309/01.ajg.0001148088.65641.b3
Primary Topic
Fungal Infections and Studies
Type
article
Field-Weighted Citation Impact
0.00
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article

S5157 Coccidioidal Peritonitis: A Rare Manifestation of Disseminated Coccidioidomycosis

The American Journal of Gastroenterology
Fungal Infections and Studies
article

S5157 Coccidioidal Peritonitis: A Rare Manifestation of Disseminated Coccidioidomycosis

article en

Abstract

Introduction: Disseminated coccidioidomycosis, primarily a pulmonary process, can rarely extend to extrapulmonary sites with significant morbidity. Peritoneal involvement is atypical and may mimic peritoneal carcinomatosis. In endemic regions, coccidioidal peritonitis should be in the differential of patients presenting with vague abdominal symptoms, weight loss, and imaging with omental caking and ascites. Risk factors include immunocompromise and living in regions of dry climates with dusty conditions. Comprehensive evaluation can necessitate imaging, serology, and histopathology. Case Description/Methods: A 55-year-old man from Southern California’s desert valley region presented with several months progressive abdominal discomfort and unintentional weight loss. Computed tomography (CT) imaging of the chest revealed a spiculated pulmonary nodule with mediastinal lymphadenopathy; abdominal CT revealed a diffusely thickened peritoneum, ascites, and omental caking. Diagnostic paracentesis revealed high protein and low serum-ascites albumin gradient concerning for peritoneal carcinomatosis. Given the patient's geographical history and imaging findings serologic testing for Coccidioides was ordered, revealing elevated IgM and IgG titers. Coccidioides complement fixation testing was also positive with a titer of 1:512, supportive of a diagnosis of disseminated coccidioidomycosis. A subsequent biopsy of an infected neck epidermal cyst revealed granulomatous inflammation with large spherules containing endospores consistent with coccidioidomycosis, further supporting the diagnosis. High-dose fluconazole (800 mg daily) led to symptomatic and radiographic improvement. Discussion: While disseminated coccidioidomycosis represents 5-10% of cases, peritoneal involvement is rare as gastrointestinal dissemination occurs in only 2.4%. In this immunocompetent patient from a Coccidiomycosis endemic region, though the initial imaging findings suggested malignancy, a high index of suspicion for this infection led to his appropriate work up and eventual diagnosis. High-dose fluconazole therapy (800 mg daily) has been reported to be effective in disseminated disease. Early recognition and treatment is important to minimize morbidity and mortality. This case of coccidiodal peritonitis highlights the need for awareness to include fungal infections in the differential for patients living in endemic areas where coccidioidomycosis can masquerade as malignancy.

The American Journal of GastroenterologyVol. 120(10S2)
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Fungal Infections and Studies
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