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Systemic sclerosis associated with colliquative necrosis in the cerebellum
Alessandro Ricci1, Hambra Di Vitantonio2, Danilo De Paulis1
1Department of Neurosurgery, San Salvatore city Hospital, L'Aquila, Italy.
Surgical Neurology International
|May 9, 2017
Summary
Systemic sclerosis (SS) can cause rare cerebellar lesions. This case highlights ischemic necrosis in the cerebellum, mimicking a brain abscess, in a patient with scleroderma.
Area of Science:
- Neurology
- Rheumatology
- Pathology
Background:
- Scleroderma is a complex autoimmune collagen disorder affecting multiple organs (systemic sclerosis, SS) or skin only (localized scleroderma, LS).
- Neurological manifestations of scleroderma are rare, with cerebellar involvement being exceptionally uncommon.
Observation:
- A 56-year-old male presented with cerebellar lesions that mimicked a brain abscess.
- Surgical excision revealed histopathological findings of ischemic necrosis due to vasculopathy.
Findings:
- Bacteriological and viral tests were negative.
- Rheumatologic tests were consistent with a scleroderma pattern.
- This case represents a rare instance of SS causing cerebellar colliquative necrosis.
Implications:
- This report adds to the limited literature on scleroderma affecting the posterior cranial fossa.
- Understanding the pathogenetic mechanisms, clinical presentations, and radiological features of scleroderma-induced cerebellar necrosis is crucial for diagnosis and management.

