Skull Base Enchondroma and Chondrosarcoma in Ollier Disease and Maffucci Syndrome.
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DOI: 10.1016/j.wneu.2019.06.087
Abstract: BACKGROUND Maffucci syndrome (MS) and Ollier disease (OD) are rare diseases characterized by multiple benign enchondromas. Incidence of skull base (SB) enchondromas and the risk of malignant transformation remain unknown. Most SB lesions are asymptomatic… read more here.
Keywords: observation; ollier disease; enchondroma chondrosarcoma; skull base ... See more keywords
Images in Vascular Medicine: Clinical and radiological features of Maffucci syndrome
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DOI: 10.1177/1358863x221101654
Abstract: A 26-year-old woman presented with extensive bluish violet nodules on both hands and feet. She reported gradual asymmetric growth on the whole body over the last 20 years, which seriously affected her daily life. Informed… read more here.
Keywords: medicine clinical; clinical radiological; medicine; maffucci syndrome ... See more keywords
Surgical Resection Combined with Sclerotherapy Treating Maffucci Syndrome’s Venous Malformation in Head and Neck Region
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DOI: 10.1177/15385744221140687
Abstract: Purpose: Here, we report our experience treating a patient with Maffucci syndrome and evaluate the outcomes resulting from surgical management combined with sclerotherapy in the treatment of head and neck venous malformations (VMs). A 19-years-old… read more here.
Keywords: combined sclerotherapy; region; maffucci syndrome; head neck ... See more keywords
Sclerosing angiomatoid nodular transformation of the spleen in a patient with Maffucci syndrome: a case report and review of literature
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DOI: 10.1186/s13000-017-0670-z
Abstract: BackgroundMaffucci syndrome is a congenital, non-hereditary mesodermal dysplasia characterized by multiple enchondromas and hemangiomas. The presence of visceral vascular lesions in this syndrome is exceedingly rare.Case presentationWe report a 26-year-old female who was diagnosed with… read more here.
Keywords: nodular transformation; angiomatoid nodular; case; sclerosing angiomatoid ... See more keywords
A Rare Co-Occurrence of Maffucci Syndrome and Astrocytoma with IDH1 R132H Mutation: A Case Report
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DOI: 10.3390/medicina59061056
Abstract: Background: Maffucci syndrome is a rare genetic disorder associated with the development of multiple enchondromas and soft tissue cavernous hemangiomas, as well as an increased risk of malignant tumors. Case Description: Here we report a… read more here.
Keywords: idh1; occurrence maffucci; report; case ... See more keywords