# A Case of Rectal Malakoplakia Associated With Crohn’s Disease: An Incidental Finding

**Authors:** Jean C Lafontaine Álvarez, Gabriela Portilla Skerret, María J Marcos Martínez, Rafael Rodríguez López

PMC · DOI: 10.7759/cureus.84829 · Cureus · 2025-05-26

## TL;DR

A rare case of rectal malakoplakia in a Crohn’s disease patient on immunosuppressive therapy is reported, highlighting the importance of histology for accurate diagnosis.

## Contribution

This paper presents a rare clinical case linking rectal malakoplakia with Crohn’s disease under immunosuppressive treatment.

## Key findings

- Rectal malakoplakia was diagnosed in a 28-year-old female with Crohn’s disease on infliximab.
- Histopathology confirmed the presence of Michaelis-Gutmann bodies and CD68-positive histiocytes.
- The patient was successfully managed with ciprofloxacin while continuing immunosuppressive therapy.

## Abstract

Malakoplakia is a rare granulomatous disorder characterized by defective phagolysosomal activity in macrophages and the presence of Michaelis-Gutmann (MG) bodies, often affecting immunosuppressed individuals. Although it most frequently involves the genitourinary tract, gastrointestinal involvement - particularly in the rectum and sigmoid colon - has been documented. We report a rare case of rectal malakoplakia in a 28-year-old female with penetrating ileocolonic Crohn’s disease (CD) on infliximab. During surveillance colonoscopy, distal rectal mucosal nodularity, erythema, and friability were noted. Histopathology showed foamy histiocytes containing periodic acid Schiff-positive, diastase-resistant MG bodies, and CD68 confirmed histiocytic origin. A diagnosis of rectal malakoplakia was rendered, and the patient was managed with ciprofloxacin while continuing immunosuppressive therapy and a scheduled follow-up colonoscopy.

Malakoplakia may mimic malignancy or inflammatory bowel disease clinically and endoscopically, making histologic evaluation essential for accurate diagnosis. Escherichia coli is the most commonly implicated organism, and fluoroquinolones are typically effective treatments. Surgical intervention is generally reserved for refractory cases. This case highlights the need to consider malakoplakia in the differential diagnosis of atypical rectal lesions in immunosuppressed patients, including those with CD, to ensure timely and appropriate management.

## Linked entities

- **Chemicals:** ciprofloxacin (PubChem CID 2764)
- **Diseases:** Crohn’s disease (MONDO:0005011), malakoplakia (MONDO:0018913)

## Full-text entities

- **Genes:** CD68 (CD68 molecule) [NCBI Gene 968] {aka GP110, LAMP4, SCARD1}
- **Diseases:** rectal lesions (MESH:D012002), erythema (MESH:D004890), malignancy (MESH:D009369), granulomatous disorder (MESH:D006105), CD (MESH:D003424), inflammatory bowel disease (MESH:D015212), Malakoplakia (MESH:D008287)
- **Chemicals:** ciprofloxacin (MESH:D002939), fluoroquinolones (MESH:D024841), infliximab (MESH:D000069285)
- **Species:** Homo sapiens (human, species) [taxon 9606], Escherichia coli (E. coli, species) [taxon 562]

## Full text

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## Figures

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## References

14 references — full list in the complete paper: https://tomesphere.com/paper/PMC12189029/full.md

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Source: https://tomesphere.com/paper/PMC12189029