Results 91 to 100 of about 30,638 (241)

Mesenchymal Hamartoma Mimicking Hepatoblastoma

International Journal of Organ Transplantation Medicine, 2014
Mesenchymal hamartoma and hepatoblastoma are common causes of hepatic masses in pediatric population; they have similar radiologic and pathologic features.
A Bahador, B Geramizadeh, M Rezazadeh Kermani, S Moslemi   +3 more
doaj  

Importance of NAB2-STAT6 Fusion in the Diagnosis of Pancreatic Solitary Fibrous Tumor with Hamartoma-Like Features: A Case Report and Review of the Literature

Case Reports in Pathology, 2015
We report a case of pancreatic hamartoma-like solitary fibrous tumor which was differentiated from pancreatic hamartoma with the detection of NAB2-STAT6 fusion, a specific mutation for solitary fibrous tumors.
Kei Tanaka, Takashi Kishimoto, Masayuki Ohtsuka, Yukio Nakatani, Masaru Miyazaki   +4 more
doaj   +1 more source

Multidisciplinary surgical management of Cowden syndrome: report of a case [PDF]

, 2016
Cowdenâ s Syndrome (CS) is a rare congenital autosomal dominant disorder that affects around 1/200000 patients with an incomplete penetrance and variable expressivity, characterized by alterations in a tumor suppressor gene. A 14-year-old Caucasian male
Gallenzi, Patrizia, Patini, Romeo, Staderini, Edoardo   +2 more
core   +1 more source

Kisspeptin as a test of hypothalamic dysfunction in pubertal and reproductive disorders

Andrology, Volume 14, Issue 4, Page 1002-1016, May 2026.
Abstract The hypothalamic–pituitary–gonadal axis is regulated by the gonadotropin‐releasing hormone pulse generator in the hypothalamus. This is comprised of neurons that secrete kisspeptin in a pulsatile manner to stimulate the release of GnRH, and, in turn, downstream gonadotropins from the pituitary gland, and subsequently sex steroids and ...
Aureliane C. S. Pierret, Aaran H. Patel, Elisabeth Daniels, Alexander N. Comninos, Waljit S. Dhillo, Ali Abbara   +5 more
wiley   +1 more source

Seromucinous hamartoma with unique clinical and histopathological features: a case report and review of the literature

Journal of Medical Case Reports
Background We present this case to highlight the importance of considering seromucinous hamartoma in the differential diagnosis of nasal cavity lesions, particularly due to its rarity and potential for being mistaken for more aggressive pathologies ...
Mikhael Makhoul, Nadim Khoueir, Myriam Khneisser, Hussein Nassereddine   +3 more
doaj   +1 more source

A Case Series of Sudden Death in Children Aged 12 Months to 4 Years From LPIN1 Deficiency and PPA2 Deficiency in Queensland

Journal of Paediatrics and Child Health, EarlyView.
Sophie Manoy, Sally Smith, Marita Smith, Catherine Atthow, Janette Spicer, Matthew Lynch, Michelle Lipke, Julie A. McEniery, David Coman, Anita Inwood, Jim McGill, Carolyn Bursle   +11 more
wiley   +1 more source

Acral Mesenchymal Spindle Cell Neoplasm With a Novel HMGA2::NCOA2 Fusion

Journal of Cutaneous Pathology, Volume 53, Issue 5, Page 402-406, May 2026.
ABSTRACT Molecular profiling has revolutionized the field of soft tissue pathology, enhancing diagnostic precision and treatment strategies. The integration of molecular analysis and immunohistochemistry has been crucial for classifying diagnostically challenging acral mesenchymal neoplasms.
Grace Z. Armstrong, Carina A. Dehner, Eitan Halper‐Stromberg, Esther Baranov, Anna C. Eden, Rachel P. Kowal   +5 more
wiley   +1 more source

HYBRID SCINTIGRAPHY OF RARE SPLENIC HAMARTOMA

Journal of Cancer and Allied Specialties, 2018
Splenic hamartoma, also known as splenoma, splenic adenoma or nodular hyperplasia, is a rare benign splenic tumor. It is composed of disordered vascular channels with abnormal mixture of red or white splenic pulp.
Mairah Razi, Humayun Bashir, Zia Salman Faruqui   +2 more
doaj   +1 more source

Multilocular Cystic Nephroma – A Surgical and Radiological Dilemma [PDF]

, 2011
Multilocular cystic nephroma is a slow growing benign renal tumor. It has been identified as exclusive adult lesion, more common in females. It commonly occurs as an asymtomatic mass, occasionally with hematuria.
Anil Malleshi Betigeri , Boopathi subramaniyam, Int J Cur Bio Med Sci.
core  

Giant Pulmonary Hamartoma in a Child: A Case Report

Journal of Paediatrics and Child Health, EarlyView.
Jurgen Schleef, Marianna Carbi, Valentina Kiren, Marco Rabusin, Sergio Ghirardo, Massimo Maschio, Egidio Barbi, Rossana Bussani, Claudio Granata, Anita Spezzacatene   +9 more
wiley   +1 more source