Uterine Haemangioma in Klippel–Trenaunay–Weber Syndrome
نویسندگان
چکیده
منابع مشابه
Glomeruloid haemangioma and POEMS syndrome.
A 49-year-old milkman presented after the acute onset of blurred vision, anorexia, malaise, weight loss and ankle swelling. There was also a 4-month history of progressive dyspnoea, weakness, parasthesiae, tinnitus and hearing loss and earlier nerve conduction studies had revealed a demyelinating peripheral neuropathy. After a normal CT scan, undertaken because the patient had papilloedema, the...
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We describe two patients with haemangioma with thrombocytopenia (Kasabach-Merritt syndrome). Both were treated with corticosteroids without notable improvement. The first patient responded satisfactorily to radiotherapy, whereas the second showed a slow spontaneous resolution.
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A 29 year old Chinese female who presented with spontaneous purpura, was found to have gross hepatomegaly and thrombocytopenia. The thrombocytopenia responded to steroid therapy but relapsed when the dose of steroid was tapered down. Subsequent investigations revealed that the hepatomegaly was due to a large haemangioma of her liver. For symptomatic hepatic haemangioma, surgical excision is the...
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The Klippel-Trenaunay syndrome (KTS) is a rare syndrome characterised by the triad of varicose veins, bony and soft tissue hypertrophy, and cutaneous haemangioma. A 30 year old man with KTS with a right mediastinal mass which progressively enlarged over 5 years is described. Computed tomography, magnetic resonance imaging, and bronchial angiography revealed a vascular lesion in the azygous area...
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Cavernous haemangioma of uterine cervix is very rare benign vascular tumor. Less than 50 cases have been reported till date, amongst them only few cases are associated with pregnancy.Although it is rare but may cause gynaecological and obstetrical complications.Cavernous haemangioma of cervix mainly managed by surgical excision.A multiparous lady at 37weeks pregnancy presented with complaints o...
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ژورنال
عنوان ژورنال: Journal of the Royal Society of Medicine
سال: 1988
ISSN: 0141-0768,1758-1095
DOI: 10.1177/014107688808101118