Results 91 to 100 of about 57,842 (313)

Dermatologic Features of Endocrine Tumor Syndromes—Systematic Review and Meta‐Analysis

International Journal of Dermatology, EarlyView.
ABSTRACT Endocrine tumor syndromes, including multiple endocrine neoplasia types 1, 2A, and 2B (MEN1, MEN2A, MEN2B), Carney complex (CNC), and PTEN hamartoma tumor syndrome (PHTS), are hereditary conditions characterized by multisystem tumor development.
Sára Pálla, Zseraldin Metyovinyi, Fanni Adél Meznerics, Arash Mirzahosseini, Judit Tőke, Miklós Tóth, Henriett Butz, Attila Patócs, Márta Medvecz   +8 more
wiley   +1 more source

هامارتوم کندروييد قفسه سينه در نوزادی: گزارش يک مورد نادر [PDF]

, 2010
مقدمه: هامارتوم کندروييد قفسه سينه، تومور خوش ­خيم بسيار نادری است که معمولاً هنگام تولد يا در ابتدای دوران کودکی بروز مي­يابد. اين بيماری غالباً به­صورت يک توده قابل لمس در جدار قفسه سينه تظاهر مي­يابد.
جهانگيری, فریبا, خالصی, نسرین, فرشته‌نژاد, سید محمد, گوهردهی, گلنار   +3 more
core  

PTEN hamartoma tumor syndromes in childhood: description of two cases and a proposal for follow-up protocol [PDF]

, 2013
PTEN hamartoma tumor syndromes (PHTS) are a spectrum of hamartomatous overgrowth syndromes associated with germline mutations in the tumor suppressor PTEN gene located on 10q23.3.
Antona, V, CORSELLO, Giovanni, CUPIDO, Francesco, Fragapane, T, Giachino, D, PICCIONE, Maria   +5 more
core   +1 more source

Cutaneous Ciliated Cyst of the Ear

Pediatric Dermatology, EarlyView.
ABSTRACT Cutaneous ciliated cysts are rare benign lesions initially observed exclusively in the lower extremities of young females. Since their first descriptions, there have been numerous case reports of the entity occurring in males and females, in varying anatomical locations. Here, we present a case of cutaneous ciliated cyst reported for the first
Allan Fong, Andrew H. Huang, Jonathan Bush   +2 more
wiley   +1 more source

Five Cases of Hepatic Mesenchymal Tumors Diagnosed by Endoscopic Ultrasound‐Guided Tissue Acquisition

DEN Open, Volume 6, Issue 1, April 2026.
ABSTRACT Percutaneous biopsy remains the gold standard for diagnosing focal liver lesions; however, endoscopic ultrasound‐guided tissue acquisition (EUS‐TA) has recently emerged as a promising alternative. Although its diagnostic performance is favorable, most available evidence has focused on epithelial tumors, and reports on mesenchymal tumors are ...
Yuichi Takano, Naoki Tamai, Jun Noda, Tetsushi Azami, Fumitaka Niiya, Tatsuya Yamagami, Akihiro Nakamura, Genshu Tate, Takafumi Ogawa, Masatsugu Nagahama   +9 more
wiley   +1 more source

Hamartoma mesenquiamal hepático m crianças: relato de dois casos. [PDF]

, 2003
Trabalho de Conclusão de Curso - Universidade Federal de Santa Catarina, Centro de Ciências da Saúde, Departamento de Pediatria, Curso de Medicina, Florianópolis ...
Prestes, Fábio Xavier
core  

Double‐chambered left ventricle in a pediatric patient with tuberous sclerosis complex: A case report

Pediatric Investigation, EarlyView.
Haoxuan Li, Yufei Xie, Qun Wu, Xiaomin Duan, Fangyun Wang, Xin Zhang, Jing Wang   +6 more
wiley   +1 more source

Identification of BCL2L11 as a Candidate Gene for Hereditary Predisposition to Non‐Medullary Thyroid Cancer Using Familial Whole‐Exome‐Sequencing

Clinical Genetics, Volume 109, Issue 3, Page 458-469, March 2026.
Whole‐exome sequencing of five families with non‐medullary thyroid cancer revealed three candidate genes. Functional analyses confirmed BCL2L11 as a strong candidate gene for hereditary predisposition to non‐medullary thyroid cancer. ABSTRACT Familial non‐medullary thyroid cancer, defined as two or more affected first‐degree relatives, accounts for 3 ...
Duygu Abbasoglu, Mathis Lepage, Nicolas Sonnier, Sandrine Viala, Nancy Uhrhammer, Flora Ponelle‐Chachuat, Anne Cayre, Maud Privat, Mathias Cavaillé, Yannick Bidet   +9 more
wiley   +1 more source

An extremely rare case of neuromuscular and vascular hamartoma of the appendix

Surgical Case Reports, 2020
Background Neuromuscular and vascular hamartoma is a rare lesion of the small intestine, with only 26 cases reported since its initial description in 1982. No occurrence of hamartoma in the appendix has been reported until now.
Takahiro Sasaki, Tomohisa Furuhata, Masashige Nishimura, Tatsunori Ono, Akiyoshi Noda, Hirotaka Koizumi, Nobuyoshi Miyajima, Takehito Otsubo   +7 more
doaj   +1 more source

Polarisation‐Sensitive Optical Coherence Tomography for Surgical Margin Evaluation and Diagnosis of Excised Canine Cutaneous and Subcutaneous Tumours

Veterinary and Comparative Oncology, Volume 24, Issue 1, Page 69-79, March 2026.
ABSTRACT Intraoperative surgical margin evaluation is not routine in veterinary medicine. Polarisation‐sensitive optical coherence tomography (PS‐OCT) is a variant of spectral domain optical coherence tomography (SD‐OCT) that can provide real‐time cross‐sectional imaging of surgical margins with additional information about the polarisation of light in
Christina E. Orona, Ryan Jennings, Julianna DiMichele, Gabrielle Fontes, Carley Johnson, Jorge Santana Mignucci, Nikesh Patel, Yi‐Fan Shen, Hannah Weaver, Jocosa Yasenchack, Laura E. Selmic   +10 more
wiley   +1 more source