Authors

  • Munira S. Mahmudova
    Senior Lecturer Of The Department Internal Medicine №1 Tashkent Medical Academy, Uzbekistan
  • Surayyo M. Shukurdjanova
    Associate Professor Of The Department Internal Medicine №1 Tashkent Medical Academy, Uzbekistan
  • Nigora B. Nuritdinova
    Associate Professor Of The Department Internal Medicine №1 Tashkent Medical Academy, Uzbekistan

DOI:

https://doi.org/10.37547/TAJMSPR/Volume04Issue12-01

Keywords:

Parkes Weber syndrome venous angiodysplasia

Abstract

The article presents a clinical case of congenital arteriovenous dysplasia – Parkes Weber syndrome of the lower extremities. The features of its clinical picture and the difficulties of diagnosis are described. It is emphasized that Parkes Weber syndrome is a rare congenital disease of the vascular system, in some cases with the absence of its typical clinical manifestations and combined with other pathologies of the veins.

References

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Dan VN, Sapelkin SV. Angiodisplasii (vrogdennie poroki razvitia sosydov). Moskva: Verdana; 2008. 200 p. (Russian).

Parkes WF. Angioma formation in connection with hypertrophy of limbs and hemihypertrophy. Brit. J. Derm. Syph. 1907;19:231-237.

Sachin K, Rashmi S, Manish S, Siddhartha W, Uday L. Haemangiomas and venous malformations of the head and neck: A retrospective analysis of endovascular management in 358 patients. Indian J. Plast. Surg. 2013;46(1):109-116. doi: 10.4103/0970-0358.113727.

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