ABSTRACT :
 This case of Klippel-Trénaunay syndrome (KTS) is being shared as a clinical experience for future reference regarding the presentation and management bleeding per rectum in KTS. Bleeding potentially lethal complication due to colorectal hemangiomas rare cases Decision making choice treatment these patients subject many variables different methods medical surgical treatments hav...

Klippel-Trénaunay syndrome (KTS) is an uncommon entity. This congenital malformation is characterized by the triad of soft tissue or bony hypertrophy, cutaneous vascular malformations, and atypical venous abnormalities. We report here a case of KTS and discuss the clinical features, investigations, and management of this enigmatic condition.

A 30-month-old boy was brought in with the complaint of gradually increased size of his right lower extremity from birth. Soft tissue hypertrophy was detected in his right thigh, right dorsal region and scrotum. On the right leg, the skin had bluish discoloration. The leg was swollen and edeomatous. On plain radiography, we detected soft tissue hypertrophy, and there was length discrepancy betw...

Short neck and fusion of cervical vertebrae are observed in several genetic conditions and well-defined syndromes. An 8-year-old boy with a short neck, low-set posterior hairline, deafness and limited neck motion was suspected of having such a condition. Clinical and radiographic examination led to the diagnosis of Klippel-Feil syndrome.

OBJECTIVE To report the clinical presentation and peculiarity of management of Klippel-Feil syndrome (KFS) at the University of Abuja Teaching Hospital, Gwagwalada. BACKGROUND KFS is a rare pathology that has not been previously reported on in Nigeria. METHODS Case review was employed to report this pathology. RESULT This case is a 10 year old boy with KFS presenting with cosmetic blemish...

Klippel-Feil Syndrome is a complex condition due to aberrant fusion of two or more cervical vertebrae characterised by short neck, low hairline, facial asymmetry and limited neck movement. Mandibular hypoplasia, submucous cleft, congenitally missing teeth, asymmetries mouth breathing are frequently observed in patients with Syndrome. Management symptomatic supportive which necessitates multidis...

We read with great interest the article written by Alomari et al, and agree with the authors that Klippel-Trenaunay syndrome is not associated with spinal cord AVM. However, in their discussion, in relationship to spinal cord AVM with Parkes Weber syndrome, they comment briefly that “Spinal AVM has not been reported to be a feature of Parkes Weber syndrome.” Here, we demonstrate a case of Parke...

A 44-year-old man with no relevant past medical history was referred for colonoscopy because of recurrent hematochezia and iron deficiency anemia. He reported no abdominal pain or weight loss. He had been on oral therapy with ferrous sulfate. A hypertrophic lower left limb was seen on physical examination. Colonoscopy (●" Video1) revealed ectasia and congestion of the submucosal and mucosal ves...