Context: Perineuriomas are rare tumors composed of cells resembling those of the normal perineurium. It usually occurs in subcutaneous, soft-tissue or intraneural locations. Very few reports in the literature have described perineuriomas in the gastrointestinal tract, including the stomach, colon and jejunum.
Case Report: We report the clinicopathological and immunohistochemical features of a case of ileal perineurioma that was manifested clinically as intestinal obstruction due to intussusception. Ileal perineurioma has not previously been reported at this anatomical location.
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http://dx.doi.org/10.1590/s1516-31802011000100010 | DOI Listing |
Rev Esp Enferm Dig
May 2024
Interventional Radiology Center, Xiangya Hospital Central South University, .
Neurofibromatosis type I is a relatively rare inherited disorder. Simultaneous occurrence of abdominal tumors of three types in NF-I and causing intussusception is rare. We report a synchronous case of small bowel gastrointestinal stromal tumor, small bowel adenocarcinoma, and ganglioneuroma complicated by intussusception in an old woman with NF-I.
View Article and Find Full Text PDFAm J Case Rep
August 2023
Department of Diagnostic Radiology, University of Puerto Rico School of Medicine, San Juan, Puerto Rico.
BACKGROUND Neurofibromatosis 1 is a neurocutaneous disorder with multisystemic manifestations. When patients are lacking overt cutaneous manifestations, diagnosis may be delayed and may complicate diagnosis and management of atypical presentations of this disease. It is thus important to strive to obtain relevant and/or complete history to arrive at the appropriate diagnosis.
View Article and Find Full Text PDFMedicine (Baltimore)
January 2023
Department of Pathology, College of Medicine, Chosun University, Gwangju, Korea.
Rationale: Type 1 neurofibromatosis (NF1) is one of the most prevalent genetic conditions. NF1 is characterized by cutaneous plexiform neurofibromas and café au lait skin pigmentation, and is inherited in an autosomal dominant trait with mutation in the neurofibromin 1 gene on chromosome 17. Neurofibromin is involved in Ras proto-oncogene regulation.
View Article and Find Full Text PDFPol Arch Intern Med
February 2023
Department of Gastroenterology, Affiliated Changzhou No. 2 People’s Hospital of Nanjing Medical University, Changzhou, Jiangsu Province, China.
Acta Med Port
April 2023
Serviço de Cirurgia Geral. Unidade Local de Saúde do Litoral Alentejano. Santiago do Cacém. Portugal.
Mesenteric schwannomas are rare benign tumors that arise in the mesentery. Ileal diverticula and intestinal malrotation in adults are rare findings, since they are usually asymptomatic. We present the case of an 86-year-old man, without any known previously known medical conditions, who was admitted in the emergency department with recurrent abdominal distension and intense pain.
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