Sclerosing mesenteritis is a chronic disease that primarily affects the mesenteric adipose tissue and encompasses a range of fibrotic and inflammatory pathologies. Due to its low incidence, the etiology remains unclear, though various factors are thought to contribute to its onset. Clinical manifestations are nonspecific, ranging from asymptomatic cases to persistent abdominal pain, which is the most common symptom. Incidental findings on imaging have increased with the widespread use of computed tomography (CT) scans. However, the diagnosis remains histological. Sclerosing mesenteritis is mainly associated with a good prognosis, as it typically follows a benign clinical course and rarely presents with complications or persistent symptoms. In this article, the authors present a clinical case of an 82-year-old male patient who presented with abdominal pain, constipation, and vomiting. The patient underwent an urgent laparotomy for intestinal occlusion. Histological examination confirmed sclerosing mesenteritis. Due to its limited understanding, sclerosing mesenteritis is often misdiagnosed. It should be considered as a differential diagnosis, particularly in patients with poorly defined abdominal pain, normal laboratory studies, and nonspecific imaging findings, to avoid unnecessary treatments. Nonetheless, urgent surgical intervention may be necessary in cases presenting with intestinal occlusion or uncontrolled pain.
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http://dx.doi.org/10.7759/cureus.75235 | DOI Listing |
Cureus
December 2024
Esophagogastric Surgery, Unidade Local de Saúde (ULS) de Viseu Dão-Lafões, Viseu, PRT.
Cancer Rep (Hoboken)
December 2024
Department of Internal Medicine, Hospital St. Josef Braunau, Braunau am Inn, Austria.
Hematology Am Soc Hematol Educ Program
December 2024
Division of Hematology, University of British Columbia, Vancouver, British Columbia, Canada; and Division of Hematology, Dalhousie University, Halifax, Nova Scotia, Canada.
Immunoglobulin G4-related disease (IgG4-RD) is an immune-mediated disease with many important manifestations in hematopoietic and lymphoid tissue. IgG4 is the least naturally abundant IgG subclass, and the hallmark feature of IgG4-RD is markedly increased IgG4-positive plasma cells (with an IgG4 to IgG ratio >40%) in affected tissue, along with elevated polyclonal serum IgG and IgG4 in most patients. Histological diagnosis is essential, and other key features include storiform fibrosis, lymphoplasmacytic infiltrate, tissue eosinophilia, and obliterative phlebitis.
View Article and Find Full Text PDFCureus
September 2024
Department of Gastroenterology, Toyonaka Municipal Hospital, Toyonaka, JPN.
A 57-year-old male with a history of hypertension, diabetes mellitus, and dyslipidemia was found to have elevated carcinoembryonic antigen (CEA) levels during a routine health checkup, leading to an abdominal computed tomography (CT) scan. The scan identified a mesenteric mass with an irregular morphology. Subsequent blood tests indicated no signs of inflammation, and follow-up CEA levels normalized.
View Article and Find Full Text PDFRev Med Chil
November 2023
Departamento de Radiología, Hospital San Juan de Dios, Santiago, Chile.
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