Multi-organ pyoderma gangrenosum presenting as refractory prostatitis

We report a rare case of concurrent cutaneous and prostatic pyoderma gangrenosum (PG) in a man in his 70s. The patient initially presented with dysuria, pelvic discomfort and a boggy prostate, consistent with bacterial prostatitis. Despite prolonged antibiotic therapy, his symptoms progressed and imaging revealed a prostatic abscess. Following transurethral resection of the prostate, he developed painful necrotic ulcers across the trunk and extremities. Histopathological examination of both the prostate and skin demonstrated sterile neutrophilic inflammation, consistent with PG. Dermatology initiated systemic corticosteroids, mycophenolate mofetil and infliximab, resulting in partial disease control. This case highlights a unique presentation of simultaneous visceral and cutaneous PG in the absence of prior trauma or surgery and underscores the importance of considering non-infectious neutrophilic dermatoses in patients with refractory prostatitis and evolving systemic inflammation.

Authors

Institutions

Publication Details

Journal
BMJ Case Reports
Published
2025-12-01
DOI
https://doi.org/10.1136/bcr-2025-269359
Primary Topic
Autoimmune and Inflammatory Disorders
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Multi-organ pyoderma gangrenosum presenting as refractory prostatitis

Kristan Schiele, Dylan J. Badin, Lawrence M. Dagrosa, Shaofeng Yan et al.
BMJ Case Reports
Autoimmune and Inflammatory Disorders
article

Multi-organ pyoderma gangrenosum presenting as refractory prostatitis

Kristan Schiele, Dylan J. Badin, Lawrence M. Dagrosa, Shaofeng Yan, Alicia T. Dagrosa, Ayushya Ajmani
article en

Abstract

We report a rare case of concurrent cutaneous and prostatic pyoderma gangrenosum (PG) in a man in his 70s. The patient initially presented with dysuria, pelvic discomfort and a boggy prostate, consistent with bacterial prostatitis. Despite prolonged antibiotic therapy, his symptoms progressed and imaging revealed a prostatic abscess. Following transurethral resection of the prostate, he developed painful necrotic ulcers across the trunk and extremities. Histopathological examination of both the prostate and skin demonstrated sterile neutrophilic inflammation, consistent with PG. Dermatology initiated systemic corticosteroids, mycophenolate mofetil and infliximab, resulting in partial disease control. This case highlights a unique presentation of simultaneous visceral and cutaneous PG in the absence of prior trauma or surgery and underscores the importance of considering non-infectious neutrophilic dermatoses in patients with refractory prostatitis and evolving systemic inflammation.

BMJ Case ReportsVol. 18(12)
Dartmouth College (US), Dartmouth–Hitchcock Medical Center (US)
Good health and well-being
Openalex Percentile: Top 29%
Autoimmune and Inflammatory Disorders
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.