Purpose: We discuss the coexistence of Klippel–Trénaunay–Weber syndrome with various malignancies, the possible
histogenetic pathways and therapeutic implications

Aygencel G

Benno Kusters

Bruart J

De Simone C

Fay A

Howitz P

Jacky De Rooy

Lezama-del Valle P

Maciej Pruszczynski

Marieke J. M. Ploegmakers

Mentzel T

Oettler WJ

René P. H. Veth

Rossi S

Spallone A

WeissSW

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English

A case of primary hemangiopericytoma associated with Klippel– Tre ´naunay–Parker–Weber syndrome.

A huge malignant degenerating neurofibroma of the lower leg coexistent with type 1 Recklinghausen disease. Dtsch Med Wochenschr

A variant of the Klippel– Tre ´naunay–Weber syndrome with temporal lobe astrocytoma. Acta Paediatr Scand

Angiosarcoma arising in hemangioma/ vascular malformation of four cases and review of the literature.

Angiosarcoma of soft tissue.

Hodgkin disease in patient with Klippel–Tre ´naunay syndrome.

Intraneural angiosarcoma and angiosarcoma arising in benign and malignant peripheral nerve sheath tumours: Clinicopathological and immunohistochemical analysis of four cases.

Klippel–Tre ´naunay syndrome and rhabdomyosarcoma in a 3-year-old. Arch Ophtalmol

La Quaglia MP. Malignant vascular tumors in young patients.

Simultaneous occurrence of aneurysm and multiple meningioma in Klippel–Tre ´naunay patients: Case report. Surg Neurol

Squamous cell carcinoma in a venous ulcer as a complication of the Klippel–Tre ´naunay syndrome. Clin Exp Dermatol

Angiosarcoma With Malignant Peripheral Nerve Sheath Tumour
Developing in a Patient With Klippel–Trénaunay–Weber Syndrome