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http://dx.doi.org/10.1111/jocd.15743 | DOI Listing |
Ann Afr Med
September 2025
Department of Medical Gastroenterology, Dr. D. Y. Patil Vidyapeeth, Dr. D. Y. Patil Medical College, Hospital and Research Centre, Pune, Maharashtra, India.
Solitary rectal ulcer syndrome (SRUS) is an uncommon, benign condition that presents with a wide range of symptoms mimicking other pathological conditions, often leading to misdiagnosis and delays in treatment. A 60-year-old male patient was diagnosed with SRUS with rectal stricture with the help of colonoscopy, anorectal manometry, magnetic resonance defecography, and histopathological examination. He was managed with high-fiber diet, laxatives, biofeedback therapy, argon plasma coagulation, and stricture dilatation, which effectively alleviated the patient's condition.
View Article and Find Full Text PDFSurg Case Rep
September 2025
Department of Pathology, Self-Defense Forces Central Hospital, Tokyo, Japan.
Introduction: Solitary fibrous tumor (SFT) is a rare mesenchymal neoplasm that most commonly originates in the pleura but can also occur at extrapleural sites, including the abdominal cavity. Among these, primary SFT of the stomach is exceptionally rare. Due to overlapping clinical, endoscopic, and radiologic characteristics, distinguishing SFT from gastrointestinal stromal tumor (GIST) can be particularly challenging.
View Article and Find Full Text PDFInherited bone marrow failure syndrome 1 (IBMFS1) is a rare autosomal dominant disorder associated with mutations in the SRP72 gene. However, mutations in this gene are exceedingly rare, and the clinical manifestations are often nonspecific, leading to delayed or misdiagnosed cases. The incidence, lifetime risk, and clinical management guidelines for SRP72-related IBMFS1 are poorly understood due to its rarity.
View Article and Find Full Text PDFCureus
August 2025
Internal Medicine, St Luke's Hospital, Easton, USA.
Streptococcal toxic shock syndrome (STSS) is a rare but life-threatening illness characterized by rapid progression to multi-organ failure. This is a case of a middle-aged male patient who initially presented with localized chest wall pain, erythema, vomiting, and diarrhea. These nonspecific symptoms rapidly progressed to systemic shock and multi-organ dysfunction, including acute kidney injury, pleural effusions, demand ischemia of the heart, and the development of a characteristic diffuse, sunburn-like rash.
View Article and Find Full Text PDFMedicine (Baltimore)
September 2025
Department of Obstetrics and Gynecology, Electric Power Teaching Hospital, Capital Medical University, Beijing, China.
Rationale: Cotyledonoid dissecting leiomyoma (CDL) is an exceptionally rare and morphologically unusual benign uterine leiomyoma. Its malignant-mimicking radiographic and intraoperative features pose a significant diagnostic challenge, often leading to misinterpretation and potentially overtreatment. This case is reported for its rarity and to highlight the critical importance of pathological recognition.
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