A Case of Infantile Myofibromatosis.
- Author:
Hong Tak LEE
;
Seung Ho CHANG
;
Tae Young YOON
- Publication Type:Case Report
- Keywords:
Infantile myofibromatosis
- MeSH:
Actins;
Desmin;
Female;
Fibroblasts;
Follow-Up Studies;
Humans;
Infant, Newborn;
Myocytes, Smooth Muscle;
Myofibroblasts;
Myofibromatosis*;
Necrosis;
Parturition;
Pericytes;
Thorax
- From:Korean Journal of Dermatology
1997;35(1):182-186
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
Infantile myofibromatosis is an uncornmon, benign, self-limiting, localized or generalized process, probably of hamartomatous origin, which consists to a large degree of cells having the characteristics of myofibroblasts and sometimes of pericytes. Both solitary and multicentric forms occur. Most lesions are present at birth or in early infancy, and some are familial in origin. A female newborn presented with a firm, round, red colored, 3 x 3 cm sized tumor with central necrosis on the left chest. Histological examination revealed well-circumscribed nodules consisting of short bundles of plump, spindle shaped cells displaying staining characteristics intermediate between fibroblasts and smooth muscle cells. The tumor was immunoreactive for actin but did not stain for desmin. A Follow-up examination at the age of 3 months revealed a moderate degree of spontaneous regressior of the lesion.
