Results 111 to 120 of about 30,430 (219)

Nonimmune hydrops fetalis and bilateral pulmonary hypoplasia in a newborn infant with nuchal vascular hamartoma

The Turkish Journal of Pediatrics, 1997
Nuchal vascular hamartoma was found in a newborn premature infant who presented with nonimmune hydrops fetalis, pulmonary hypoplasia due to bilateral pleural effusion and polyhydramnios in utero.
H Ozkan, H Gülen, N Demir, E Ozer, S Haberal, D Erçal, N T Cevik   +6 more
doaj  

Hamartoma, Pituitary

, 2017
Hamartomas are congenital malformations composed of a heterotopic mass of neurosecretory neurons, fiber bundles and glial cells, frequently associated with true precocious puberty, usually occurring before 3 years of age. They can be associated with laughter or generalized tonic-clonic seizures, mental retardation, behavioral disturbances and ...
Patti, G., Morana, G., Di Iorgi, N., Maghnie, M.   +3 more
openaire   +2 more sources

A rare cause of bronchial obstruction: Endobronchial hamartoma case report

Radiology Case Reports
Most of the pulmonary endobronchial lesions are malignant in origin. In rare instances, benign lesions such as endobronchial hamartoma may be the cause of the endobronchial tree obstruction.
Zineb Bouanani, Asmae Raïs, Fatima Zahra Benbrahim, Amal Akammar, Nizar El Bouardi, Meryem Haloua, Youssef My Alaoui Lamrani, Meryem Boubbou, Mounia Serraj, Bouchra Amara, Marouane Lakranbi, Yassine Ouadnouni, Mohammed Smahi, Mustapha Maaroufi, Badreddine Alami   +14 more
doaj   +1 more source

Orthotopic Liver Transplantation for Benign Hepatic Neoplasms [PDF]

, 1995
Iwatsuki, S, Madariaga, JR, Selby, R, Starzl, TE, Tepetes, K, Webb, M   +5 more
core   +1 more source

Pulmonary hamartoma

Zdravniški Vestnik, 2006
Background: Hamartomas are the most common benign neoplasms of the lung. The population incidence is 2.5/1000. In most cases the diagnosis is based on computed tomography (CT) and fine needle aspiration biopsy (FNAB).
Jerca Blazina, Izidor Kern, Igor Požek, Stanko Vidmar   +3 more
doaj  

Síndrome de Cowden: a propósito de una familia afectada [PDF]

, 2006
El síndrome de Cowden es una rara genodermatosis caracterizada por múltiples hamartomas ubicados en tejidos y órganos diversos derivados de las tres hojas embrionarias. Las manifestaciones clínicas de la enfermedad de Cowden se explican especialmente por
Blanco, Verónica, keochgerián, Verónica   +1 more
core   +1 more source

Imaging diagnosis-imaging and histopathologic characteristics of a vertebral hamartoma in a cat: Vertebral Hamartoma in a Cat [PDF]

, 2018
Alexander, Benoit, Cordy, Corzo-Menendez, Kloc, Martin-Vaquero, Middleton, Morris, Njoku, Padgett, Parkes, Sanders, Sanders, Smith, Stalin, Summers, Wells, Wilson, Zaki   +18 more
core   +2 more sources

Nasal anomalies review with CT or MRI: from congenital to malignant. [PDF]

, 2014
Learning Objectives. To describe imaging findings of a wide spectrum of uncommon nasal cavity masses evaluated at our institution by CT, CBCT and MR imaging, clinically and pathologically proven. Background.
GAGLIARDO, Cesare, LA TONA, Giuseppe, LO CASTO, Antonio, LO RUSSO FRANCESCO, PURPURA, Pierpaolo, SPECIALE, Riccardo   +5 more
core  

A comparative immunohistochemical study of Ki-67 expression in adenomatoid odontogenic tumour, unicystic ameloblastoma and dentigerous cyst [PDF]

, 2014
Magister Chirurgiae Dentium - MChDThe aim of this study was to investigate the biological profile oftheAOT by comparing the Ki-67 proliferative indices of the AOT, Unicystic Ameloblastoma (UA) and Dentigerous Cyst (DC) using ImmunoRatio® software ...
Fakir, E
core  

Nasal tissue-derived hamartoma in the maxillary gingiva of a calf [PDF]

, 2016
Hinako Tanaka, Kazuo Azuma, Norihiko Ito, Shinji Kono, Takehito Morita, Takeshi Tsuka, Tomohiro Imagawa, Tomohiro Osaki, Yoshiharu Okamoto, Yusuke Murahata   +9 more
core   +1 more source