Results 51 to 60 of about 14,994 (170)

Hepatic Epithelioid Hemangioendothelioma [PDF]

, 2020
The paper gives a clinical example of diagnosing hepatic epithelioid hemangioendothelioma. With allowance made for that the tumor occurs rarely (less than 1% of cases of all vascular tumors), the authors provide the clinical example to demonstrate the ...
I. S. Skrynnikov, M. N. Sorokin, A. A. Ugrimov, I. Z. Korobkova, I. V. Kirsan', D. A. Dremin, S. M. Kakalov   +6 more
core   +1 more source

Epithelioid Hemangioendothelioma in the Tongue: A Rare Case Report

Türk Patoloji Dergisi, 2023
Epithelioid hemangioendothelioma is a rare malignant vascular neoplasm caused by the proliferation of neoplastic endothelial cells. Epithelioid hemangioendothelioma may develop in any organ, but it is commonly observed in the extremities. The tongue is a
Deniz SURMELI CIRKIN, Ilke Evrim SECINTI, Esin DOGAN, Gul SOYLU OZLER   +3 more
doaj   +1 more source

Pink Polypoid Papulo‐Vesicles on Labia Majora

JEADV Clinical Practice, EarlyView.
Maria Chiara Mercuri, Michela Tabanelli, Silvia Zago, Diego Abbenante   +3 more
wiley   +1 more source

Hippo pathway at the crossroads of stemness and therapeutic resistance in breast cancer

Molecular Oncology, Volume 20, Issue 7, Page 1667-1693, July 2026.
Dysregulation of the Hippo pathway drives nuclear accumulation of YAP/TAZ, activating stemness‐related transcriptional programs that sustain breast cancer stemness and fuel therapeutic resistance across subtypes, underscoring Hippo signaling as a targetable vulnerability. Figure created and edited with BioRender.com.
Giulia Schiavoni, Antonella Palmese, Stefano Scalera, Laura Cipriani, Davide Mascolo, Patrizia Vici, Teresa Arcuri, Lorena Filomeno, Eriseld Krasniqi, Giovanni Blandino, Giulia Bon, Marcello Maugeri‐Saccà   +11 more
wiley   +1 more source

Dermoscopy of kaposiform hemangioendothelioma: a case report

Dermatology Reports
Kaposiform hemangioendothelioma (KHE) is a rare vascular tumor of infancy, characterized by an infiltrative, firm, and ill-defined plaque that may be associated with Kasabach-Merritt phenomenon.
Filomena Barbato, Maria Maddalena Nicoletti, Gaetano Licata, Eugenia Veronica Di Brizzi, Giuseppe Argenziano, Caterina Mariarosaria Giorgio   +5 more
doaj   +1 more source

Epithelioid hemangioendothelioma of the temporal artery presenting as temporal arteritis: Case report and literature review

Rare Tumors, 2009
Hemangioendotheliomas are classified as epithelioid hemangioendothelioma(EHE), retiform hemangioendothelioma, composite hemanioendothelioma, Kaposiform hemangioendothelioma (with or without Kasabach-Merritt syndrome), and Spindle cell ...
Salem Alowami, Ahmed Nasr, Dina El Demellawy   +2 more
doaj   +1 more source

A subset of high‐grade sarcomas with myogenic differentiation are associated with recurrent FGFR fusions

The Journal of Pathology: Clinical Research, Volume 12, Issue 4, July 2026.
Abstract Recurrent fusions involving FGFR1‐4 genes have been previously described in rare subsets of mostly benign chondroid and mesenchymal neoplasms involving bone and soft tissue. However, a more comprehensive analysis of sarcomas associated with FGFR fusions, including their incidence and histotypes, has not been performed.
Maximus CF Yeung, Carla Saoud, Sarah Chiang, Meera Hameed, Cristina R Antonescu   +4 more
wiley   +1 more source

Pulmonary Epithelioid Hemangioendothelioma-Mimicking Mesothelioma

, 2020
Pulmoner epithelioid hemangioendothelioma is a rare and multifocal malignant tumor of vascular origin. Patients are generally asymptomatic. Chest pain, cough, weight loss, hemoptysis, and pleural effusion are seen in symptomatic patients. Moreover, it
Tolga Semerkant, ESME, HIDIR, ÜNLÜ, YAŞAR, SEMERKANT, TOLGA, Hıdır Esme, Zeynep Bayramoglu, BAYRAMOĞLU, ZEYNEP, Yasar Unlu   +7 more
core   +1 more source

Painful Purplish Lesion on the Right Lower Lip Mucosa

Oral Diseases, EarlyView.
Isabella Cristine Pegolo Dos Santos Alamino, Hilton M. A. Hicz, Alan Grupioni Lourenço, Joel D. B. Padua, Leandro Dorigan de Macedo, Lara Maria Alencar Ramos Innocentini   +5 more
wiley   +1 more source

Congenital Atrophic Dermatofibrosarcoma Protuberans: A Case Report and Narrative Review of the Literature

Clinical Case Reports, Volume 14, Issue 7, July 2026.
ABSTRACT Dermatofibrosarcoma protuberans is a rare dermal and subcutaneous soft‐tissue tumor, uncommon in children, characterized by CD34 positivity and COL1A1‐PDGFB fusion. Prognosis is generally good, but local recurrence risk is high, so complete excision with clear margins and six‐monthly follow‐up for three years after surgery is recommended in ...
Sima Shamshiri Khamene, Izat Mohammad Khawajah, Taha Shahbazi, Safoura Shakoei   +3 more
wiley   +1 more source