Macrodystrophia Lipomatosa: Radiologic-Pathologic Correlation

Author:

Upadhyay Deepika1,Parashari Umesh C2,Khanduri Sachin2,Bhadury Samarjit2

Affiliation:

1. Department of Pathology, SG Post Graduate Institute of Medical Sciences, Lucknow, UP, India

2. Department of Radio Diagnosis, Era's Lucknow Medical College, Lucknow, UP, India

Abstract

Macrodystrophia lipomatosa (MDL) is a rare cause of congenital macrodactyly, characterised by progressive proliferation of all mesenchymal elements, with disproportionate increase in fibro-adipose tissue. It occurs most frequently in lower limbs along the distribution of the medial plantar nerve. MDL presents as localised gigantism of the hand or foot and comes to clinical attention for cosmetic reasons, mechanical problems secondary to degenerative joint disease, or development of neurovascular compression. Here, we report a case of MDL, with altered soft tissue growth due to an earlier surgery, making clinical diagnosis difficult. However, with a complete radio-clinical work-up and review of the history, a provisional diagnosis of MDL was made, which was confirmed by histopathology and during surgery.

Publisher

Scientific Scholar

Subject

Radiology, Nuclear Medicine and imaging

Reference9 articles.

1. Pathology of macrodactyly;Desai;Bull Hosp Jt Dis Orthop Inst,1990

2. Congenital macrodactyly: A clinical study;Syed;Acta Orthop Belg,2005

3. Local gigantism (a manifestation of neurofibromatosis): Its relation to general gigantism and to acromegaly illustrating the influence of intrinsic factors in disease when development of the body is abnormal;Inglis;Am J Pathol,1950

4. Clinical analysis of 73 cases of macrodactyly;Wu;Zhonghua Wai Ke Za Zhi,2008

5. Macrodystrophia lipomatosia: A case report;Ozturk;Acta Orthop Traumatol Turc,2004

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