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1.
Rev. argent. dermatol ; 104: 91-100, ene. 2023.
Article Dans Espagnol | LILACS-Express | LILACS | ID: biblio-1535516

Résumé

RESUMEN El Síndrome de Parkes Weber se caracteriza por sobrecrecimiento de una extremidad asociado a malformación capilar, venosa, linfática y arteriovenosa. Se presenta el caso de una paciente de 23 años de edad que acudió al Servicio de Dermatología por presentar una úlcera de novodesarrollada sobre malformación capilar congénita.Nos fue posible arribar al diagnóstico utilizando diversos estudios de imágenes, mientras que la medida terapéutica, con el carácter de profilaxis terciaria, consistió en embolizaciones múltiples.


SUMMARY Parkes Weber Syndrome is characterized by overgrowth of a limb with capillary, venous, lymphatic, and arteriovenous malformation. We present the case of a 23-year-old patient who came to the dermatology service for an ulcer on congenital capillary malformation.We were able to arrive at the diagnosis using various imaging studies, while the therapeutic measure, with the character of tertiary prophylaxis, consisted of multiple embolizations.

2.
J. vasc. bras ; 20: e20210075, 2021. graf
Article Dans Anglais | LILACS | ID: biblio-1287077

Résumé

Abstract Varicose veins of the lower limbs are common. However, pulsatile varicose veins are unusual. They could be an indicator of a sinister underlying pathology, such as severe cardiac dysfunction. It is easy to miss these rare cases during clinical workup, which can result in futile treatment with potentially dangerous consequences. In this report, we describe 2 cases of pulsatile varicose veins that highlight different etiologies and management strategies for this condition.


Resumo Varizes dos membros inferiores são comuns. Entretanto, varizes pulsáteis são raras, podendo ser indicadoras de uma patologia subjacente sombria como disfunção cardíaca grave. É fácil deixar passar esses casos raros durante exames clínicos, o que pode resultar em tratamento fútil com consequências potencialmente perigosas. Neste relato, descrevemos dois casos de varizes pulsáteis que evidenciam as diferentes etiologias e estratégias de manejo para essa condição.


Sujets)
Humains , Mâle , Femelle , Adulte d'âge moyen , Sujet âgé , Varices/diagnostic , Écoulement pulsatoire , Insuffisance tricuspide/complications , Varices/étiologie , Varices/thérapie , Syndrome de Sturge-Weber/complications , Inutilité médicale
3.
Vascular Specialist International ; : 165-169, 2019.
Article Dans Anglais | WPRIM | ID: wpr-762023

Résumé

A 58-year-old male patient with severe claudication due to thrombosis of the left ilio-femoro-popliteal artery aneurysm. He also had a venous stasis ulcer with a history of multiple embolotherapy of arteriovenous malformation. Duplex sonography revealed reflux and varicose veins of the left great saphenous vein (GSV). A sequential bypass surgery was performed that consisted of excision of the left external iliac and common femoral artery aneurysm, external iliac to deep femoral interposition with an expanded polytetrafluoroethylene graft, and femoro-posterior tibial artery bypass with the reversed left GSV. Symptoms of claudication were alleviated and the chronic ulcer was healed in time. To our knowledge, this is the first report of successful bypass in a patient with arterial aneurysm, arteriovenous malformation, and venous insufficiency that can be diagnosed as an atypical case of Parkes Weber syndrome. Long-term follow-up is needed to define the fate of aneurysms and varicose vein graft.


Sujets)
Humains , Mâle , Adulte d'âge moyen , Anévrysme , Artères , Fistule artérioveineuse , Malformations artérioveineuses , Embolisation thérapeutique , Artère fémorale , Études de suivi , Polytétrafluoroéthylène , Artère poplitée , Veine saphène , Syndrome de Sturge-Weber , Thrombose , Artères tibiales , Transplants , Ulcère , Ulcère variqueux , Varices , Insuffisance veineuse
4.
J. vasc. bras ; 16(4): 320-324, out.-dez. 2017. graf
Article Dans Anglais | LILACS | ID: biblio-954678

Résumé

Abstract Parkes-Weber syndrome is a congenital vascular disease that comprises capillary, venous, lymphatic, and arteriovenous malformations. Although Parkes-Weber syndrome is a clinically distinct entity with serious complications, it is still frequently misdiagnosed as Klippel-Trenaunay syndrome, which consists of a triad of malformations involving the capillary, venous, and lymphatic vessels, without arteriovenous fistulas. Both syndromes are generally diagnosed with Doppler ultrasound and confirmed by magnetic resonance angiography. The aim of this study is to describe one case of Klippel-Trenaunay syndrome, in a 36-year-old patient, and one case of Parkes-Weber syndrome, in a 21-year-old patient. We review the literature in order to discuss the possible causes and consequences of these diseases related to venous hypertension and angiodysplasia, taking a clearer approach to their differences, and discussing their treatment.


Resumo A síndrome de Parkes-Weber é uma doença vascular congênita que consiste em malformações capilares, venosas, linfáticas e arteriovenosas. Embora seja uma entidade clinicamente distinta com complicações graves, essa síndrome ainda é frequentemente diagnosticada erroneamente como síndrome de Klippel-Trenaunay, que consiste em uma tríade de má formação nos vasos capilares, venosos e linfáticos, sem fístula arteriovenosa. Ambas as síndromes são geralmente diagnosticadas através de ultrassom Doppler e confirmadas pela angiografia por ressonância magnética. O objetivo deste estudo é descrever um caso de síndrome de Klippel-Trenaunay em um paciente de 36 anos de idade e um caso de síndrome de Parkes-Weber em uma paciente de 21 anos. A literatura foi revisada com o objetivo de discutir as possíveis causas e consequências dessa doença e sua associação à hipertensão venosa e angiodisplasia. O presente trabalho também levanta discussão a respeito das diferenças sintomatológicas de ambas as síndromes e seus respectivos tratamentos.


Sujets)
Humains , Mâle , Femelle , Adulte , Jeune adulte , Syndrome de Sturge-Weber/imagerie diagnostique , Syndrome de Klippel-Trénaunay/imagerie diagnostique , Malformations artérioveineuses , Syndrome de Sturge-Weber/complications , Syndrome de Sturge-Weber/thérapie , Syndrome de Klippel-Trénaunay/complications , Syndrome de Klippel-Trénaunay/thérapie , Diagnostic différentiel
5.
Medisan ; 20(10)oct. 2016. ilus
Article Dans Espagnol | LILACS, CUMED | ID: lil-797508

Résumé

Se describe el caso clínico de una infante de 4 años de edad atendida inicialmente en el Servicio de Pediatría del Hospital el Instituto Ecuatoriano de Seguridad Social de Ibarra, de la Repúblicade Ecuador y luego en el de Cirugía Vascular, donde se le diagnosticó síndrome de Parkes Weber.


The case report of a 4 years child is described assisted initially in the Pediatrics Service of the Social Security Ecuadorian Institute Hospital of Ibarra in Ecuador Republic and then in the Vascular Surgery Service, where she was diagnosed Parkes Weber syndrome.


Sujets)
Syndrome de Sturge-Weber , Syndrome de Klippel-Trénaunay , Enfant d'âge préscolaire
6.
Chinese Journal of Dermatology ; (12): 812-814, 2014.
Article Dans Chinois | WPRIM | ID: wpr-468657

Résumé

A girl who aged eight years and seven months presented with prunosus patches on the right buttock for 8 years,gradual unilateral enlargement of the right lower limb for more than 7 years,and multiple vegetations for 1 year.Dermatological examination showed nevus flammeus and multiple malodorous vegetations over the right lower limb with high skin temperature.The right lower limb was thicker and longer than the left lower limb.X-ray examination,magnetic resonance imaging and Doppler ultrasound examination revealed high-flow vascular malformations.Pathological examination of the vegetations showed vascular proliferation,fibroblast proliferation and erythrocyte extravasation.She was diagnosed as Parkes-Weber syndrome accompanied by pseudo-Kaposi's sarcoma.

7.
Insuf. card ; 5(3): 150-153, sep. 2010. ilus
Article Dans Espagnol | LILACS | ID: lil-633381

Résumé

Se presenta el caso de un paciente joven con fístula arterio-venosa congénita en miembro superior derecho, que evoluciona con elefantiasis del miembro afectado, miocardiopatía dilatada e insuficiencia cardíaca de alto gasto. Ante el fracaso del tratamiento quirúrgico (ligadura de la fístula), se decide la embolización percutánea de la misma.


We present a case of a young patient with congenital arteriovenous fistula in the right upper limb, which evolves with elephantiasis of the affected limb, dilated cardiomyopathy and high output heart failure. With the surgical treatment failure (fistula ligation), we decided the fistulas embolization.


Relatamos o caso de um jovem paciente com fístula artério-venosa congênita no membro superior direito, que evolui com elefantíase do membro afetado, cardiomiopatia dilatada e insuficiência cardíaca de alto débito. Com o fracasso do tratamento cirúrgico (ligadura de fistula), decidiu-se a embolização da fístula.

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