S6238 When Inflammation Mimics Malignancy: A Case of Idiopathic Sclerosing Mesenteritis

Introduction: Idiopathic sclerosing mesenteritis is a rare condition with an estimated global prevalence of <1%. Radiological imaging of idiopathic sclerosing mesenteritis can have features very similar to carcinoid tumors. We present a case where patient suspected to have carcinoid tumor based on imaging findings was eventually found to have idiopathic sclerosing mesenteritis on histopathology. Case Description/Methods: An 80-year-old woman with history of paroxysmal atrial fibrillation, OSA, congestive heart failure, recent mitral valve repair, pulmonary hypertension, anxiety, depression and seizure disorder presented with intractable nausea. Computed tomography abdomen and pelvis found a partially calcified mesenteric mass in the mid left abdomen, measuring 49 mm. A subsequent magnetic resonance imaging (MRI) abdomen showed a 4.2 × 3.8 cm left abdominal nodular mesenteric mass, bowel wall thickening and desmoplastic reaction, aligning with the diagnosis of a carcinoid tumor. Consequently, the patient underwent exploratory laparotomy with resection of mesenteric mass along with segment of small bowel. Histopathology report of this mesenteric mass revealed no malignant cells but rather showed mesenteric fibrosis, calcification and plasma cell infiltration. Overall, the findings were most consistent with sclerosing mesenteritis. Further workup was carried out to rule out common conditions associated with sclerosing mesenteritis. Autoimmune workup and immunoglobulin G4 level turned out to be negative. Pan scan also did not show any evidence of malignancy. In this context, a diagnosis of idiopathic sclerosing mesenteritis was established. Discussion: Sclerosing mesenteritis is a chronic inflammatory condition that most commonly affects the mesentery of small intestine and is characterized by inflammation, fibrosis and necrosis of mesentery. It is a rare condition most commonly seen in white men in fifth to seventh decade of life. Although definitive diagnosis requires biopsy, imaging is an important modality to diagnose sclerosing mesenteritis. In this case, MRI initially raised concern for carcinoid tumor based on imaging findings, including a nodular mass, bowel wall thickening, and desmoplastic reaction, features that can be present in both conditions (carcinoid tumor and sclerosing mesenteritis). This case highlights the importance of considering other uncommon diagnosis based on imaging findings.

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Publication Details

Journal
The American Journal of Gastroenterology
Published
2025-10-01
DOI
https://doi.org/10.14309/01.ajg.0001153412.46626.c0
Primary Topic
IgG4-Related and Inflammatory Diseases
Type
article
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article

S6238 When Inflammation Mimics Malignancy: A Case of Idiopathic Sclerosing Mesenteritis

Usama Sakhawat, Mustafa Sajjad Cheema, Ahmed Shehadah, Khandokar A. Talib et al.
The American Journal of Gastroenterology
IgG4-Related and Inflammatory Diseases
article

S6238 When Inflammation Mimics Malignancy: A Case of Idiopathic Sclerosing Mesenteritis

Usama Sakhawat, Mustafa Sajjad Cheema, Ahmed Shehadah, Khandokar A. Talib, Ali Marhaba, Abdul Subhan Talpur, Fawad Talat, Abdul Basit Khan
article en

Abstract

Introduction: Idiopathic sclerosing mesenteritis is a rare condition with an estimated global prevalence of <1%. Radiological imaging of idiopathic sclerosing mesenteritis can have features very similar to carcinoid tumors. We present a case where patient suspected to have carcinoid tumor based on imaging findings was eventually found to have idiopathic sclerosing mesenteritis on histopathology. Case Description/Methods: An 80-year-old woman with history of paroxysmal atrial fibrillation, OSA, congestive heart failure, recent mitral valve repair, pulmonary hypertension, anxiety, depression and seizure disorder presented with intractable nausea. Computed tomography abdomen and pelvis found a partially calcified mesenteric mass in the mid left abdomen, measuring 49 mm. A subsequent magnetic resonance imaging (MRI) abdomen showed a 4.2 × 3.8 cm left abdominal nodular mesenteric mass, bowel wall thickening and desmoplastic reaction, aligning with the diagnosis of a carcinoid tumor. Consequently, the patient underwent exploratory laparotomy with resection of mesenteric mass along with segment of small bowel. Histopathology report of this mesenteric mass revealed no malignant cells but rather showed mesenteric fibrosis, calcification and plasma cell infiltration. Overall, the findings were most consistent with sclerosing mesenteritis. Further workup was carried out to rule out common conditions associated with sclerosing mesenteritis. Autoimmune workup and immunoglobulin G4 level turned out to be negative. Pan scan also did not show any evidence of malignancy. In this context, a diagnosis of idiopathic sclerosing mesenteritis was established. Discussion: Sclerosing mesenteritis is a chronic inflammatory condition that most commonly affects the mesentery of small intestine and is characterized by inflammation, fibrosis and necrosis of mesentery. It is a rare condition most commonly seen in white men in fifth to seventh decade of life. Although definitive diagnosis requires biopsy, imaging is an important modality to diagnose sclerosing mesenteritis. In this case, MRI initially raised concern for carcinoid tumor based on imaging findings, including a nodular mass, bowel wall thickening, and desmoplastic reaction, features that can be present in both conditions (carcinoid tumor and sclerosing mesenteritis). This case highlights the importance of considering other uncommon diagnosis based on imaging findings.

The American Journal of GastroenterologyVol. 120(10S2)
Openalex Percentile: Top 44%
IgG4-Related and Inflammatory Diseases
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