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CASE REPORT
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Solitary intraspinal juvenile xanthogranuloma in an infant


 Department of Pathology, Topiwala National Medical College and B. Y. L. Nair Hospital, Mumbai, Maharashtra, India

Correspondence Address:
Shruti Shribhagwan Singhal,
C-wing, Flat No. 701, Sai Shradha Bldg., Phase-1, Ashokvan, Borivali, Mumbai - 400 066, Maharashtra
India
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Source of Support: None, Conflict of Interest: None

Juvenile xanthogranuloma (JXG) is a benign, non-Langerhans cell histiocytic proliferative disorder. We report a case of solitary JXG in an infant presenting as an intraspinal mass. Awareness of this mode of presentation is very important as subsequent prognosis differs from other tumors at the same location. JXG is a self-limiting dermatologic disorder usually occurring in first two decades of life. On rare occasion, it has been reported at extra-cutaneous sites such as central nervous system (CNS), eyes, liver, spleen, lungs and kidneys, and in other age groups. Isolated CNS involvement is extremely rare, especially in the spinal cord.


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    -  Shenoy A
    -  Singhal SS
    -  Shinde S
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