Volume : VII, Issue : V, May - 2018
Klippel-Trenaunay-Weber syndrome Presenting as Recurrent Rectal Bleed and Anaemia: A Rare Case Report
Dr. Saket Goel, Dr. Deepak Govil, Dr. Kalpit Goriwal
Abstract :
KlippelTrenaunay Syndrome (KTS) is a rare congenital nonhereditary syndrome of vascular malformations and soft tissue and bone hypertrophy. Though the involvement of gastrointestinal tract (GI) is uncommon in KTS, it can be a source of life–threatening bleed with a high morbidity and mortality rates. We here report a case of a 26 year old gentleman, already a diagnosed case of KTS, who presented to us with recurrent GI bleed and anaemia necessitating blood transfusions every 20 days. This case report aims to highlight the management protocols for this rare presentation of the syndrome.
Keywords :
KlippelTrenaunay Syndrome naevusvasculosusosteohypertrophicus angioosteohypertrophy syndrome hemangiectatic hypertrophy.
Article:
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DOI : 10.36106/ijsr
Cite This Article:
Dr. Saket Goel, Dr. Deepak Govil, Dr. Kalpit Goriwal, Klippel–Trenaunay–Weber syndrome Presenting as Recurrent Rectal Bleed and Anaemia: A Rare Case Report, INTERNATIONAL JOURNAL OF SCIENTIFIC RESEARCH : Volume-7 | Issue-5 | May-2018
Number of Downloads : 251
References :
Dr. Saket Goel, Dr. Deepak Govil, Dr. Kalpit Goriwal, Klippel–Trenaunay–Weber syndrome Presenting as Recurrent Rectal Bleed and Anaemia: A Rare Case Report, INTERNATIONAL JOURNAL OF SCIENTIFIC RESEARCH : Volume-7 | Issue-5 | May-2018
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