Results 21 to 30 of about 1,168,856 (161)

Pioglitazone inhibits growth of carcinoid cells and promotes TRAIL-induced apoptosis by induction of p21(waf1/cip1) [PDF]

open access: yes, 2001
Background/Aims: We investigated the effect of the peroxisome proliferator-activated receptor-gamma (PPAR-gamma) agonist pioglitazone on growth and TRAIL-induced apoptosis in carcinoid cells.
Göke, Burkhard   +4 more
core   +1 more source

Malignancy within a Tail Gut Cyst: A Case of Retrorectal Carcinoid Tumour [PDF]

open access: yes, 2014
Purpose. Tailgut cysts with malignant transformation are rare entities. We discuss the diagnostic strategy and treatment of a malignancy within a tailgut cyst. Methods.
Abukar, AA   +23 more
core   +1 more source

Carcinoid tumors of the lung: A report of 11 cases

open access: yesAsian Journal of Surgery, 2013
Objective: Carcinoid tumors of the lung are rare, and account for 1% of all primary tumors of the lung. This study was undertaken to investigate the histological characteristics and clinical behavior of carcinoid tumors of the lung.
Yoshinobu Ichiki   +3 more
doaj   +1 more source

An unusual 7 cm large typical carcinoid managed by surgery: a rare case report [PDF]

open access: yes, 2020
Carcinoid tumors of the lung are uncommon group of pulmonary neoplasms. Most common site is gastrointestinal tract followed by lungs. Typical pulmonary carcinoids are usually small as described in various case series size of a typical carcinoid may ...
Firdaus, Huma   +3 more
core   +1 more source

Typical Laryngeal Carcinoid Recurrence and its Management by Conservative Surgery

open access: yesPhilippine Journal of Otolaryngology Head and Neck Surgery, 2010
Objective: Recurrence of a typical laryngeal carcinoid is extremely rare after surgery with tumor-free margins on histopathology. We present a rare case of typical laryngeal carcinoid that recurred after eight years and was managed by conservative ...
Syed Majid Hussain, Rauf Ahmad
doaj   +1 more source

Diagnosis and Therapy of Bronchopulmonary Carcinoid Tumors

open access: yesChinese Journal of Lung Cancer, 2011
Bronchopulmonary carcinoid tumors are relatively uncommon neoplasms and typically benign and slow growing. However, more aggressive subtypes may develop early nodal and distant metastases.
Sen WEI, Xin LI, Jun CHEN, Qinghua ZHOU
doaj   +1 more source

Atelectasis in pediatrics: a case of carcinoid tumor

open access: yesRare Tumors, 2017
Carcinoid pulmonary tumors occur in the fourth to sixth decades of life. Usually, typical carcinoid arise a decade earlier when compared to atypical carcinoid (45 years and 55 years, respectively).
Cláudia Guerreiro   +4 more
doaj   +1 more source

An unusual clinical manifestation of a relapsed typical pulmonary carcinoϊd tumor

open access: yesRespiratory Medicine Case Reports, 2021
Typical carcinoid tumors of the lungs carry an excellent prognosis after complete surgical excision. However, recurrence of these cancers remains poorly described in the literature and may occur many years after surgery.We report a case of carcinoid ...
Nidhal Belloumi   +6 more
doaj   +1 more source

European Standard Clinical Practice Guideline and EXPeRT Recommendations for the Diagnosis and Management of Gastroenteropancreatic Neuroendocrine Neoplasms in Children and Adolescents

open access: yesPediatric Blood &Cancer, EarlyView.
ABSTRACT Pediatric gastroenteropancreatic neuroendocrine neoplasms (GEP‐NENs) are extremely rare and clinically heterogeneous. Management has largely been extrapolated from adult practice. This European Standard Clinical Practice Guideline (ESCP), developed by the EXPeRT network in collaboration with adult NEN experts, provides (adult) evidence ...
Michaela Kuhlen   +23 more
wiley   +1 more source

Bronchoscopic treatment of intraluminal typical carcinoid: A pilot study [PDF]

open access: yes, 1998
Objective: The curative potential of various bronchoscopic treatments such as Nd:YAG laser, photodynamic therapy, and brachytherapy for the treatment of intraluminal tumor has been reported previously.
Postmus, Pieter E.   +4 more
core   +1 more source

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