Systemic sclerosis is a connective tissue disorder of unknown etiology. Although it is a multisystemic disorder, skin thickening is considered as a hallmark of the disease. It usually involves the lungs, gastrointestinal, and musculoskeletal systems. However, a rare subset of systemic sclerosis, systemic sclerosis sine scleroderma, is characterized by internal organ involvement and positive serologic markers with the total or partial absence of cutaneous manifestations. We present a rare association of osteopetrosis in a case of systemic sclerosis sine scleroderma, in a 22-year-old male patient, who presented with pulmonary symptoms as his chief complaints, unreported so far in literature.
CITATION STYLE
Pati, S. K., Raja, P., Behera, A. K., Ranganath, T. G., & Bodhey, N. K. (2021). Osteopetrosis in a Patient of Systemic Sclerosis Sine Scleroderma: A Rare Association. Indian Journal of Radiology and Imaging, 31(4), 1019–1022. https://doi.org/10.1055/s-0041-1740506
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