Results 61 to 70 of about 5,608,032 (152)

Perivascular epithelioid cell tumor (PEComa) of the uterine cervix associated with intraabdominal "PEComatosis": A clinicopathological study with comparative genomic hybridization analysis

open access: yesWorld Journal of Surgical Oncology, 2004
Background The World Health Organization recently recognized a family of neoplasms showing at least partial morphological or immunohistochemical evidence of a putative perivascular epithelioid cell (PEC) differentiation.
Ma Linglei   +7 more
doaj   +1 more source

Diagnostic Challenges in Choroid Plexus Tumours

open access: yesNeuropathology and Applied Neurobiology, Volume 52, Issue 4, August 2026.
In this review, we summarise the diagnostic spectrum of choroid plexus tumours, highlight key age‐dependent differential diagnoses across infants, children/adolescents and adults, and outline how histopathology, immunohistochemistry and molecular profiling support accurate tumour classification.
Christian Thomas, Martin Hasselblatt
wiley   +1 more source

Management and Outcomes of Uterine Smooth Muscle Tumour of Uncertain Malignant Potential (STUMP)

open access: yesCancer Medicine, Volume 15, Issue 7, July 2026.
ABSTRACT Background Uterine smooth muscle tumours of uncertain malignant potential (STUMP) is a mesenchymal tumour which does not fulfil the criteria for leiomyoma, benign histological subtypes, or leiomyosarcoma. The risk factors for recurrence and the rates of recurrence vary amongst different studies; as a result, there are currently no consensus ...
Aaron Hey Yin Chan   +3 more
wiley   +1 more source

Perivascular epithelioid cell

open access: yes, 1996
Description of a new cell type: Perivascular epithelioid ...
Bonetti F.   +3 more
core   +1 more source

Unveiling the mystery of hepatic epithelioid angiomyolipoma: A unique case report with literature review

open access: yesSAGE Open Medical Case Reports
Hepatic epithelioid angiomyolipoma is a rare mesenchymal liver tumor within the perivascular epithelioid cell tumor family, known for its uncertain malignancy and potential for aggressive behavior.
Da Teng   +3 more
doaj   +1 more source

A Case Report of Malignant Perivascular Epithelioid Cell Tumors of the Uterus and Literature Review [PDF]

open access: yes
Daifeng Hu,1,* Mengyue Miao,1,* Hui Zhou,1 Xia Gu,1,2 Xuedan Wang,3 Alexander Tobias Teichmann,1 Qin Wang,1 Youzhe Yang1,2 1Sichuan Provincial Center for Gynaecology and Breast Diseases, The Affiliated Hospital of Southwest Medical University ...
Teichmann AT   +7 more
core  

Perivascular Epithelioid Cell Tumor: A Case Report of a Rare Entity

open access: yes, 2021
Perivascular epithelioid cell tumor is a rare mesenchymal tumor with myomelanocytic differentiation. It mainly occurs in middle-aged females and can be found at any location.
Cardosa, MF   +4 more
core  

Microscopic endometrial perivascular epithelioid cell nodules: a case report with the earliest presentation of a uterine perivascular epithelioid cell tumor

open access: yesDiagnostic Pathology, 2012
Perivascular epithelioid cell (PEC) tumors (PEComas) are a family of related mesenchymal tumors composed of PECs which co-express melanocytic and smooth muscle markers.
Fang Chia-Lang, Lin Yun-Ho, Chen Wei-Yu
doaj   +1 more source

Perivascular epithelioid cell tumor located retroperitoneally with pulmonary lymphangioleiomyomatosis: report of a case

open access: yes, 2014
Perivascular epithelioid cell neoplasms, also known as "PEComas", are unusual mesenchymal tumors, exhibiting perivascular epithelioid cell differentiation and characterized by a mixed myogenic and melanocytic phenotype. "PEComas not otherwise specified" (
SOLAINI, LEONARDO   +4 more
core   +1 more source

Perivascular epithelioid cell tumor of the ileum: a case report

open access: yes, 2016
Perivascular epithelioid cell tumors (PEComa) are tumors of perivascular epithelioid cells with immunohistochemical features of smooth muscle and melanocytic tumors. The PEComa of the gastrointestinal tract is rare.
Mora-Soler,Ana María   +6 more
core   +1 more source

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