2014, Number 609
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Rev Med Cos Cen 2014; 71 (609)
Neoplasia endocrina múltiple tipo 1
González LEA, Mora HGA
Language: Spanish
References: 10
Page: 29-33
PDF size: 166.03 Kb.
ABSTRACT
The term Multiple Endocrine
Neoplasia (MEN), was
implemented in 1968. It refers
to a disorder with synchronous
or metachronous neoplasms
in two or more different
endocrine organs. It may occur
sporadically or hereditary, in
the last case usually occurs in
several members of a family for
generations. MEN is divided
into several types, the most
prevalent are types 1 and 2,
(10) type 2 was sub classified
into 2A and 2B in 1975. (5)
Currently there are genetic
methods that allow identifying
existing mutations and this can
better determine its diagnosis,
prognosis and treatment.
REFERENCES
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Callender, G; Rich, T; Perrier, N. Multiple Endocrine Neoplasia Syndromes. Surgical Clinics of North American 2008. Vol. 88: 863- 895.
Larrandaburu, M et al. Neoplasia Endocrina Múltiple. Presentación de GONZÁLEZ, MORA: NEOPLASIA ENDOCRINA MÚLTIPLE TIPO 1 33 una familia afectada con diagnostic molecular. Revista Médica Uruguaya. 2008. Vol 24: 203-211.
Richards, M. Thyroid Cancer Genetics: Multiple Endocrine Neoplasia Type 2, Non-Medullary Familial Thyroid Cancer, and Familial syndromes Associated with Thyroid Cancer. Surgical Oncology Clinics of North America. 2008. Vol. 18: 39-52.
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Thakker, R. Multiple endocrine neoplasia type 1 (MEN1). Best Practice & Research Clinical Endocrinology & Metabolism 2010. Vol. 24: 355-370.
Vinik, A; Gonzalez, R. New and Emerging Syndromes due to Neuroendocrine Tumors. Endocrinology Metabolic Clinics North America 2011. Vol. 40: 19-63.
White, M; Doherty, G. Multiple Endocrine Neoplasia. Surgical Oncology Clinics of North America, 2008. Vol. 18. Pag 439-459.