2014, Number 04
<< Back Next >>
MediSan 2014; 18 (04)
Neurofibromatosis type1 in a young adult
Gámez RO, Correa SMG, Rodríguez MM, Miyares DAG, Romero CD
Language: Spanish
References: 10
Page: 596-601
PDF size: 609.35 Kb.
ABSTRACT
The case report of a 29 year-old patient with a family history of neurofibromatosis who began to notice the presence of subcutaneous soft, unpainful, disseminated tumors in the trunk and in the 4 limbs, associated with radicular pain and paresthesias, difficult walking, as well as muscle atrophy in the upper limbs is described. The results of the neurological physical examination and of biopsy allowed to diagnose this disorder.
REFERENCES
Theos A, Korf BR. Pathophysiology of neurofibromatosis type 1. Ann Intern Med. 2006;144(11):842-9.
World Heath Organization Classification of Tumors: pathology and genetics: head and neck tumors. Lyon: IARC Press; 2005.
Raymond Delacy A, Maurice V. Principles of neurology. 9 th. New York: McGraw- Hill; 2009.
Reynods RM, Brouning GGP, Nawroz I, Campbell IW. Von Recklinghausen’s neurofibromatosis type 1. Lancet. 2003;361:1552.
Wilson MA, Hillman TA, Wiggins RH, Shelton C. Jugular foramen schwanomas: diagnosis, management and outcomes. Laryngoscope. 2005;115 (8):1486-92.
Saettone León A. Neurofibromatosis segmentaria, reporte de un caso. Dermatol Perú. 2006;16(1):249-53.
Theos A, Korf BR. Pathophysiology of neurofibromatosis type 1. Ann Intern Med. 2006;144(11):842-9.
Lee MJ, Stephenson DA. Recent developments in neurofibromatosis type 1. Current Opinion in Neurology. 2007;20(2):135-41.
Obregón Mimbela J, Santillán Artolózaga A. Neurofibroma cervical gigante. Neurofibromatosis tipo 1.Comunicación de un caso clínico. An Orl Mex. 2010; 55(2):69-72.
Braunwald E. Harrison. Principios de Medicina Interna. 17 Edición. México, DF: McGraw-Hill Interamericana; 2008.