نتایج جستجو برای: secreting neoplasia

تعداد نتایج: 45603  

Journal: :the archives of bone and joint surgery 0
deep sharma department of orthopaedics, pmr block, jawaharlal institute of post graduate medical education and research (jipmer), puducherry, india pooja dhiman department of biochemistry, jipmer, puducherry, india jagdish menon department of orthopaedics, jipmer, puducherry, india komuravalli varun krishna department of orthopaedics, jipmer, puducherry, india

background:  sternocostoclavicular joint (sccj) swelling is an underdiagnosed, albeit important entity in clinical practice. the present study was conducted in order to identify the incidence and common causes of this entity.  methods:  patients presenting to the orthopaedic clinic with a swelling of the sternocostoclavicular joint, during the study period of two years were included, and detail...

Journal: :Clinical cancer research : an official journal of the American Association for Cancer Research 1998
R J Weil A O Vortmeyer S Huang R Boni I A Lubensky S Pack S J Marx Z Zhuang E H Oldfield

Pituitary adenomas may develop sporadically or as part of the multiple endocrine neoplasia type 1 (MEN 1) syndrome. The gene responsible for MEN 1 syndrome was recently identified and cloned. Low rates of MEN 1 gene mutations and deletions have been reported in sporadic pituitary adenomas. To elucidate the role of the MEN 1 gene in the pathogenesis of MEN 1-associated pituitary tumors, we exami...

Journal: :European journal of endocrinology 2004
M Rix N T Hertel F C Nielsen B B Jacobsen A S Hoejberg K Brixen J Hangaard J P Kroustrup

OBJECTIVE To describe three cases of Cushing's disease in children with multiple endocrine neoplasia type 1 (MEN1), as clinical manifestations of MEN1 are very rare in childhood. DESIGN AND METHODS A retrospective review of three cases of Cushing's disease diagnosed between 1997 and 1999. Genetic screening for MEN1 gene mutation was performed in each patient. RESULTS An ACTH-secreting micro...

Journal: :Endocrine-related cancer 2007
A Raitila M Georgitsi A Karhu K Tuppurainen M J Mäkinen K Birkenkamp-Demtröder K Salmenkivi T F Orntoft J Arola V Launonen P Vahteristo L A Aaltonen

Germline mutations in the aryl hydrocarbon receptor interacting protein (AIP) gene were recently observed in patients with pituitary adenoma predisposition (PAP). Though AIP mutation-positive individuals with prolactin-, mixed growth hormone/prolactin-, and ACTH-producing pituitary adenomas as well as non-secreting pituitary adenomas have been reported, most mutation-positive patients have had ...

Journal: :Endocrine-related cancer 2002
M L Jaffrain-Rea D Di Stefano G Minniti V Esposito A Bultrini E Ferretti A Santoro L Faticanti Scucchi A Gulino G Cantore

Pituitary tumours are usually benign neoplasia, but may have a locally aggressive or malignant evolution. This study aimed to identify factors which mostly influence their proliferative activity, in order to clarify its value for clinical and research purposes. The proliferative index was determined in a prospective series of 132 pituitary tumours as the percentage of monoclonal antibody MIB-1-...

Journal: :Revista espanola de enfermedades digestivas : organo oficial de la Sociedad Espanola de Patologia Digestiva 2015
Laura Valiente-González Teresa Martínez-Pérez Yolanda Jiménez-Martínez Raquel Martínez-Fernández Miriam Viñuelas-Chicano Carmen Julia Gómez-Ruiz José Ignacio Pérez-García Julia Morillas-Ariño Gracia Pérez-Vigara Jesús García-Cano-Lizcano Ángel Pérez-Sola

A 56-year-old woman suffered from a painful lesion in the distal phalanx of the left second finger for two months that affected both the skin and nail (Fig. 1). At the same time she presented also with hairless plate lesion in the occipital region (Fig. 2). She received antibiotics without improvement. Consequently, a biopsy was taken from the nail lesion. Histopathology showed nail infiltratio...

Journal: :Clinical chemistry 1994
E A Gerlo C Sevens

We review our data on the measurement of catecholamines and their metabolites in 19 patients with pheochromocytoma. All the assays were specific high-performance liquid chromatographic procedures with electrochemical detection. The assay of fractionated metanephrines was 100% sensitive. Normal values for both urinary norepinephrine and epinephrine were found in two asymptomatic patients with ph...

2012
Ursula Plöckinger

Multiple endocrine neoplasia type 1 (MEN-1) is a rare autosomal-dominant disease. It is associated with a broad range of endocrine tumours, most frequently arising in the parathyroid glands, the pituitary and the pancreas. Most neuroendocrine tumours will be diagnosed in the pancreas as non-functioning neuroendocrine tumours or insulinomas. Forty-two percent of the patients will develop a gastr...

Journal: :Journal of Medical Case Reports 2008
Christine Wynveen Behnaz Behmaram George Haasler Nagarjun Rao

INTRODUCTION Primary pulmonary mucinous cystic neoplasia comprises a group of tumors, from benign cystadenoma to mucinous cystadenocarcinoma. CASE PRESENTATION We report a case of primary pulmonary mucinous cystadenocarcinoma in a 75-year-old woman who was found to have a right hilar mass on a routine chest X-ray. A lobectomy was performed and the resection specimen revealed a multicystic muc...

Journal: :Veterinary journal 2010
Alexander J German Vivien H Ryan Allison C German I Stuart Wood Paul Trayhurn

Obesity is characterised by an expansion of white adipose tissue mass that can lead to adverse health effects, such as decreased longevity, diabetes mellitus, orthopaedic and respiratory disease and neoplasia. Once thought a passive fuel depot, adipose tissue is now recognised as an active endocrine organ that communicates with the brain and peripheral tissues by secreting a wide range of hormo...

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