Myoepithelial hamartoma is a very rare submucosal tumor of the stomach. Magnus-Alsleben first described 5 cases of this tumor in 1903. More recently (1993) Vandelli et al. published a review of the literature comprising only 33 cases. Histologically, the tumor is characterized by hypertrophic smooth muscle bands surrounding diverse epithelial elements that can be arranged in different ways: as a simple glandular structure, Brunner's gland, pancreatic ducts and occasionally pancreatic acinus. We report a case of myoepithelial hamartoma of the stomach simulating a gastric carcinoma.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1177/030089160709300222 | DOI Listing |
Int J Surg Case Rep
December 2024
Pathology Department, Faculty of Medicine, Mansoura University, Mansoura, Egypt.
Introduction And Importance: Periductal stromal tumors are rare breast neoplasms characterized by a unique combination of epithelial and mesenchymal tissue. Due to their infrequent occurrence, these tumors are often misdiagnosed as other breast lesions.
Case Presentation: A 47-year-old female presented with a right breast swelling.
Dig Liver Dis
May 2024
The First College of Clinical Medical Science, China Three Gorges University, Yichang, China; Institute of Digestive Disease, China Three Gorges University, Yichang, China; Department of Gastroenterology, Yichang Central People's Hospital, Yichang, China. Electronic address:
Virchows Arch
July 2024
Sikl's Department of Pathology, Faculty of Medicine in Plzen, Charles University, and University Hospital, E. Benese 13, 305 99 Pilsen , Plzen, Czech Republic.
Pancreas
August 2022
Surgery, Duke University, Durham, NC.
Pancreatic myoepithelial hamartoma is a rare, benign solid and cystic lesion of the pancreas. We present the first case of an adult with a giant myoepithelial hamartoma extending throughout the pancreas in a patient with diabetes in 4 immediate family members. The patient is a 46-year-old man presented with recurrent acute pancreatitis.
View Article and Find Full Text PDFAm J Dermatopathol
February 2022
Departamento Materno-Infantil, Universidade Federal Fluminense, Niterói, Rio de Janeiro, Brazil.
Apocrine hamartoma is a rare benign neoplasm. The histology is characterized by an excess of apocrine glands located predominantly in the reticular dermis. Pigmented apocrine hamartoma represents a histopathological variation of apocrine hamartoma containing tubules and linear cysts covered by apocrine cells on the inside with melanin and on the outside with myoepithelial cells.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!