Results 171 to 180 of about 223,917 (310)

Fuchs’ Adenoma [PDF]

Ophthalmology, 2015
Krishna R, Surapaneni, Alexander L, Ringeisen, Paul O, Phelps   +2 more
openaire   +2 more sources

Molecular Basis and Clinical Spectrum of WNT10A‐Related Oligodontia

Clinical Genetics, EarlyView.
Cellular Mechanism behind WNT10A phenotypes. ABSTRACT WNT10A mutations, a major genetic determinant of dental agenesis and ectodermal dysplasia, exert profound effects on craniofacial development. Although classified as rare disorders, these mutations account for more than half of oligodontia cases, reflecting their critical role.
Perennes Elise, Benkirane‐Jessel Nadia, Anton Nicolas, Vandamme Thierry, Clauss François, Conzatti Guillaume   +5 more
wiley   +1 more source

Prognostic value of PANOMEN-3 classification for hypopituitarism in surgically and nonoperatively managed pituitary adenomas. [PDF]

Endocr Connect
Nakhleh A, Ayada G, Assalia Naffa M, Sviri G, Zolotov S.   +4 more
europepmc   +1 more source

Adenoma Sebaceum [PDF]

Proceedings of the Royal Society of Medicine, 1932
openaire   +2 more sources

Rare Secondary Neoplasms Arising in Epidermal Nevus: A Case Series and Literature Review

Journal of Cutaneous Pathology, EarlyView.
ABSTRACT Malignant transformation is known to occur with many nevi, such as nevus sebaceus. However, cases of secondary tumors developing in an epidermal nevus (EN) are rare, with only a few case reports documented in the literature. We present three unique cases of syringocystadenoma papilliferum (SCAP), syringofibroadenoma, trichilemmoma, and basal ...
Haya A. Homsi, Melissa Piliang, Jennifer Lucas, Jennifer S. Ko, Steven D. Billings, Shira Ronen   +5 more
wiley   +1 more source

Superficial Ewing Sarcoma of the Rectum: A Case Report and the Utility of Molecular Diagnostics

Journal of Cutaneous Pathology, EarlyView.
ABSTRACT Ewing sarcoma is an undifferentiated small round cell sarcoma that most commonly presents as a malignant bone tumor in pediatric and young adult patients. The diagnosis is typically confirmed by molecular genetic identification of a fusion protein, most commonly involving members of the FET and ETS gene families.
Jessica L. Muldoon, Laura M. Warmke, Ahmed K. Alomari, Rachel P. Kowal   +3 more
wiley   +1 more source

Pouch cancer in familial adenomatous polyposis. Incidence, risk factors and literature review: a propos of three rare cases. [PDF]

Arq Bras Cir Dig
Campos FG, Martinez CAR, Moura RN, Safatle-Ribeiro AV, Marques CFS, Ribeiro Junior U, Herman P.   +6 more
europepmc   +1 more source

Skin lesion triage in organ transplant recipients using line‐field confocal optical coherence tomography: a retrospective classification study

JDDG: Journal der Deutschen Dermatologischen Gesellschaft, EarlyView.
Summary Background/objectives: Organ transplant recipients (OTRs) face an elevated risk of keratinocyte carcinomas (KC), leading to a lower threshold for biopsy. Line‐field confocal optical coherence tomography (LC‐OCT) is a non‐invasive imaging technique capable of visualizing malignant skin changes, yet its role in the management of OTRs remains ...
Kevin Jacobsen, Vinzent Kevin Ortner, Stine Regin Wiegell, Peter Alshede Philipsen, Merete Haedersdal   +4 more
wiley   +1 more source

PITUITARY ADENOMAS [PDF]

The Journal of Clinical Endocrinology & Metabolism, 1954
openaire   +2 more sources

HPV42 – a human papillomavirus classified as a low‐risk type with oncogenic potential

JDDG: Journal der Deutschen Dermatologischen Gesellschaft, EarlyView.
Summary Human papillomavirus (HPV) type 42 is a rare HPV type currently classified as “low‐risk” and belongs to the alpha genus. It has primarily been detected in benign vulvar papillomas and is predominantly associated with benign lesions such as anogenital warts.
Sven Niklas Burmann, Ulrike Wieland, Steffi Silling, Frank Oellig, David Chromy, Julia Hyun, Thilo Gambichler, Alexander Kreuter   +7 more
wiley   +1 more source