Abstract:
:Gorham-Stout syndrome (GSS) is a rare disease characterized by spontaneous and progressive osteolysis caused by benign proliferation of lymphatic vessels or capillaries. It most commonly occurs in children or young individuals without any inherited predisposition. GSS most commonly affects the shoulder girdle, pelvis, ribs and skull. Its diagnosis is mainly based on radiological and pathological findings. The present study reports on the case of a 22-year-old male patient diagnosed with GSS involving the C1-T1 vertebrae accompanied by bilateral pleural effusion. Resection of the occipital and cervical vertebral lesions and spinal reconstruction using an internal fixator were successfully performed via the posterior approach. After the surgery, the patient received bisphosphonate treatment and vitamin D supplementation. The pleural effusion gradually decreased. At the 18-month follow-up visit, no evidence of new bone obstruction was present and the patient had no neurological sequelae.
journal_name
Exp Ther Medjournal_title
Experimental and therapeutic medicineauthors
Chang KJ,Yang MH,Li B,Huang Hdoi
10.3892/etm.2020.8627subject
Has Abstractpub_date
2020-06-01 00:00:00pages
3851-3855issue
6eissn
1792-0981issn
1792-1015pii
ETM-0-0-8627journal_volume
19pub_type
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