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Indian Journal of Pathology and Microbiology
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CASE REPORT
Year : 2012  |  Volume : 55  |  Issue : 2  |  Page : 242-244

Lipofibromatosis accompanied by several congenital anomalies, report of a rare case


1 Department of Plastic and Reconstructive Surgery, Shiraz University of Medical Sciences, Shiraz, Iran
2 Department of Pathology and Transplant Research Center, Shiraz University of Medical Sciences, Shiraz, Iran

Correspondence Address:
Bita Geramizadeh
Pathology Department, Shiraz University of Medical Sciences, Shiraz, 71345-1864
Iran
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/0377-4929.97894

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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.


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