Lipofibromatosis accompanied by several congenital anomalies, report of a rare case.
Indian J Pathol Microbiol
;
2012 Apr-Jun 55(2): 242-244
Article
in English
| IMSEAR
| ID: sea-142233
ABSTRACT
Lipofibromatosis is a rare tumor of infancy, which has been reported about 10 years ago, and since then very few reports have been published. This tumor has been reported in association with congenital anomalies such as macrosyndactyly, but there is no report of multiple congenital anomalies with lipofibromatosis in the English literature as far as our knowledge goes. Herein, we report a case of this tumor associated with syndactyly, bilateral complete cleft lip and palate, trigonocephaly, and atrial septal defect.
Full text:
Available
Index:
IMSEAR (South-East Asia)
Main subject:
Congenital Abnormalities
/
Humans
/
Male
/
Tomography, X-Ray Computed
/
Face
/
Fibroma
/
Foot
/
Head
/
Histocytochemistry
/
Infant
Language:
English
Journal:
Indian J Pathol Microbiol
Year:
2012
Type:
Article
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