neoplasia

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neoplasia

[‚nē·ə′plā·zhə]
(medicine)
Formation of a neoplasm or tumor.
Formation of new tissue.
References in periodicals archive ?
Caron et al., "Pheochromocytoma in multiple endocrine neoplasia type 2: a prospective study," European Journal of Endocrinology, vol.
Immunostains for collagen type IV discriminate between C-cell hyperplasia and microscopic medullary carcinoma in multiple endocrine neoplasia, type 2a.
Palisaded encapsulated neuroma (PEN),also known as 'solitary circumscribed neuroma' is an uncommon, benign,cutaneous, neural tumor, which usually presents as small, solitary, asymptomatic, firm, skin-coloured or pink papule or nodule, usually localized on the face or close to a mucocutaneous junction.It is a disease of middle-aged adults with equal sex preponderance.It was first described by Reed et al.in 1972.Rarely, it can be multiple also but never associated with neurofibromatosis or multiple endocrine neoplasia.
Pheochromocytoma may also occur as part of Von HippelLindau disease, MEN (Multiple Endocrine Neoplasia) Syndrome Type IIA (medullary carcinoma of thyroid, pheochromocytoma, and parathyroid adenoma) or MEN IIB (medullary carcinoma of thyroid, pheochromocytoma, Marfan's and neurofibromatosis).
(September 2012) "clinical practice guidelines for multiple endocrine neoplasia type 1 (MEN1)".
(5.) Grama, D, Skogseid B, Wilander E, et al, Pancreatic tumors in multiple endocrine neoplasia type 1: Clinical presentation and surgical treatment.
Zhuang, "Multiple endocrine neoplasia 1 gene alterations in MEN1-associated and sporadic lipomas," Journal of the National Cancer Institute, vol.
They can be further divided into traumatic neuromas, palisaded and encapsulated neuromas (PEN), and mucosal neuromas associated with multiple endocrine neoplasia (MEN) 2B.
Ailment: Multiple endocrine neoplasia, type 2B Sotos has written an entire book positing that had Lincoln not been assassinated, he would have soon died from thyroid or adrenal cancer caused by this rare genetic disorder.
Its most common site is the skin presenting as multiple fibromata as part of syndrome of neurofibromatosis (von Recklinghausen's disease) or poliglandular syndrome multiple endocrine neoplasia (MEN) III [5].
Approximately 10% are malignant, and 4-8% are associated with Multiple endocrine neoplasia type 1 (MEN-1) syndrome (2).The highest incidence is in people between 40 and 60 years of age, and females show a slight predominance over males (7).
This work goes all the way back to fruit lies, good ol' Drosophila, and the authors picked a well-characterized cancer pathway: multiple endocrine neoplasia type 2 (MEN2).

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