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Metastatic myxoid round cell liposarcoma of the buttock: a case report.
Pan Afr Med J
September 2024
Department of Dermatology, Hospital Institute of Social Hygiene, Dakar, Senegal.
Article Synopsis
- Liposarcoma is a rare tumor that develops from fat tissue, commonly found in the thigh, but this case involves a tumor in the buttock of a 56-year-old man.
- The tumor, which had been present for two years, was inflammatory and ulcerated, raising concerns for other diagnoses such as squamous cell carcinoma or skin lymphoma.
- After confirming the diagnosis of myxoid round-cell liposarcoma, treatment with chemotherapy began but unfortunately led to a rapid deterioration and fatal outcome within weeks.
Estrogen Receptor Expression in DICER1-related Lesions is Associated With the Presence of Cystic Components.
Am J Surg Pathol
June 2024
Cancer Research Program, Research Institute of the McGill University Health Centre, Montreal, Canada.
Article Synopsis
Amebic Liver Abscess Complicated With a Pleural Effusion: A Case Report.
Cureus
October 2022
Internal Medicine, HCA Houston Healthcare West, Houston, USA.
Amebiasis is a fecal-oral transmitted parasitic infection caused by the protozoan and is generally seen in migrants and travelers of endemic areas. Extraintestinal infection often involves the liver, causing amebic liver abscesses. Twenty to thirty percent of these patients have pleuropulmonary involvement as a complication.
View Article and Find Full Text PDFDICER1-associated hepatic cystic neoplasm with pleuropulmonary blastoma-like features: a novel clinicopathologic diagnosis.
Mod Pathol
May 2022
Aflac Cancer and Blood Disorders Center, Children's Healthcare of Atlanta, Emory University School of Medicine, Atlanta, GA, USA.
This report documents a unique multicystic neoplasm of the liver in an 8-month-old boy with a heterozygous germline pathogenic DICER1 variant. This neoplasm, initially considered most likely a mesenchymal hamartoma based on imaging, demonstrated the characteristic histologic pattern of embryonal rhabdomyosarcoma residing in the subepithelial or cambium layer-like zone of the epithelial-lined cysts. Thus, although the differential diagnosis includes mesenchymal hamartoma, a young child with a multicystic mass lesion in the liver, lung, or kidney should both raise the possibility of a germline pathogenic DICER1 variant and also not be mistaken for one of the other hepatic neoplasms of childhood.
View Article and Find Full Text PDFPrimary Biphasic Hepatic Sarcoma in DICER1 Syndrome.
Pediatr Dev Pathol
December 2021
Department of Pathology and Laboratory Medicine, Ann & Robert H. Lurie Children's Hospital of Chicago, Chicago, Illinois.
DICER1 tumor predisposition syndrome is a rare genetic disorder that predisposes individuals to multiple benign and malignant neoplasms. The phenotype is vast and includes pleuropulmonary blastoma (PPB), thyroid nodules, cystic nephroma, Wilms tumor, ovarian Sertoli-Leydig cell tumor, and medulloepithelioma, among others. Herein, we describe a patient with a germline pathogenic variant presenting with two neoplasms that are not commonly encountered in the context of DICER1 syndrome.
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