Unusual association of two rare entities: Primary rectal linitis and Klippel-Trenaunay syndrome
<p>Klippel-Trenaunay syndrome (KTS) is a rare congenital disorder, characterized by the triad of vascular malformations (angioma), venous and or lymphatic malformations and asymmetrical disturbed growth of soft tissues and/or bone. Primary rectal linitis is a rare digestive tumor with very poo...
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Archives of Clinical Gastroenterology - Peertechz Publications,
2019-01-17.
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| LEADER | 00000 am a22000003u 4500 | ||
|---|---|---|---|
| 001 | peertech__10_17352_2455-2283_000059 | ||
| 042 | |a dc | ||
| 100 | 1 | 0 | |a Haraki I |e author |
| 700 | 1 | 0 | |a El Yazal S |e author |
| 700 | 1 | 0 | |a Ait Errami A |e author |
| 700 | 1 | 0 | |a Lairani FZ |e author |
| 700 | 1 | 0 | |a Jiddi S |e author |
| 700 | 1 | 0 | |a Samlani Z |e author |
| 700 | 1 | 0 | |a Krati K |e author |
| 700 | 1 | 0 | |a Oubaha S |e author |
| 245 | 0 | 0 | |a Unusual association of two rare entities: Primary rectal linitis and Klippel-Trenaunay syndrome |
| 260 | |b Archives of Clinical Gastroenterology - Peertechz Publications, |c 2019-01-17. | ||
| 520 | |a <p>Klippel-Trenaunay syndrome (KTS) is a rare congenital disorder, characterized by the triad of vascular malformations (angioma), venous and or lymphatic malformations and asymmetrical disturbed growth of soft tissues and/or bone. Primary rectal linitis is a rare digestive tumor with very poor prognosis. We report the case of a 41-year-old patient with Klippel trenaunay syndrome who was diagnosed with primary rectal linitis. </p> | ||
| 540 | |a Copyright © Haraki I et al. | ||
| 546 | |a en | ||
| 655 | 7 | |a Case Report |2 local | |
| 856 | 4 | 1 | |u https://doi.org/10.17352/2455-2283.000059 |z Connect to this object online. |