A Case of Neurofibromatosis with Multiple Neurofibromas on Mesentery
Journal of the Korean Pediatric Society
;
: 270-273, 1997.
Article
in Korean
| WPRIM
| ID: wpr-204728
ABSTRACT
Neurofibromatosis originally described by von-Recklinhausen in 1882, is often depicted as a chronic progressive hereditary disease characterized by pigmentation of the skin, cutaneus lesions, and numerous tumors developing in association with elements of both the central and peripheral nervous tissue. Mesenteric involvements in neurofibromatosis are very rare in childrens. We experienced a case of neurofibromatosis with multiple neurofibromas on mesentery in 6 years old male who presented with abdominal pain. The diagnosis was confirmed by clinical manifestations, abdominal CT, and histopathologic findings. Brief review of literatures was made.
Full text:
Available
Index:
WPRIM (Western Pacific)
Main subject:
Skin
/
Pigmentation
/
Tomography, X-Ray Computed
/
Abdominal Pain
/
Neurofibromatoses
/
Diagnosis
/
Genetic Diseases, Inborn
/
Mesentery
/
Neurofibroma
Type of study:
Diagnostic study
Limits:
Child
/
Humans
/
Male
Language:
Korean
Journal:
Journal of the Korean Pediatric Society
Year:
1997
Type:
Article
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