Prenatal diagnosis and hemodynamic evaluation of Klippel‐Trenaunay‐Weber syndrome

Paladini, D.; Lamberti, A.; Teodoro, A.; Liguori, M; D’Armiento, Maria; Capuano, Pasquale; Martinelli, Pasquale

doi:10.1046/j.1469-0705.1998.12030215.x

Cited by 22 publications

(13 citation statements)

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“…Although the mode of inheritance of KTTS and the risk of transmission from an affected mother to a fetus is unknown, prenatal diagnosis by ultrasound has been reported (42)(43)(44). The earliest known prospective intrauterine diagnosis of KTTS occurred at 17 weeks (43,44).…”

Section: Preconception Counselingmentioning

confidence: 99%

Klippel-Trenaunay-Type Syndrome in Pregnancy

Stein¹,

Perlow²,

Sawai³

2006

Obstetrical & Gynecological Survey

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Section: Preconception Counselingmentioning

confidence: 99%

Klippel-Trenaunay-Type Syndrome in Pregnancy

Stein¹,

Perlow²,

Sawai³

2006

Obstetrical & Gynecological Survey

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“…They belong to the group of low-flow vascular lesions and have radiologic features of both venous and lymphangial malformations. Although hemangiolymphangiomas occur relatively rarely, some cases have been reported as part of a congenital cavernous syndrome such as Klippel-Trenaunay-Weber syndrome [3]. Klippel-Trenaunay Weber syndrome is a rare congenital soft tissue anomaly characterized by the presence of multiple hemangiomas, asymmetric limb hypertrophy, and arteriovenous fistulas [3].…”

Section: Discussionmentioning

confidence: 99%

Cavernous Hemangiolymphangioma of the Testis without Cutaneous Hemangiomatosis in an Elderly Patient

et al. 2012

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Hemangiolymphangioma is an extremely rare malformation of both the lymphatic and blood vessels. To date, however, there are no reports in the literature of a hemangiolymphangioma of the testis. An 84-year-old man visited our hospital for investigation of a 1-month episode of a rapidly growing mass in his right scrotum. Scrotal ultrasonography revealed a multilobulated mass with septation in the testis. Testicular tumor markers were within the normal limit. Radical orchiectomy was performed. At surgery, a red, wide-based, nodular tumor was found on the testis. Histological examination of the resected specimen showed it to be a cavernous hemangiolymphangioma. Here we report this first case of a cavernous hemangiolymphangioma of the testis without cutaneous hemangiomatosis in an elderly patient.

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“…Another differential diagnosis of the hemangiolymphangioma is Klippel-Trenaunay-Weber syndrome. This is a rare congenital soft-tissue anomaly which is characterized by the presence of multiple hemangiomata, asymmetric limb hypertrophy and arteriovenous fistulas 13 . This syndrome has a similar ultrasonographic appearance to the vascular lesions with hemangiolymphangioma 14,15 , but the latter is not associated with asymmetric limb hypertrophy.…”

Section: Discussionmentioning

confidence: 99%