THE SYNDROME OF THE COUP DE FOUET - IS IT ALWAYS A BENIGN DISEASE

Citation
Pl. Antignani et al., THE SYNDROME OF THE COUP DE FOUET - IS IT ALWAYS A BENIGN DISEASE, Dermatologic surgery, 21(10), 1995, pp. 872-875
Citations number
14
Categorie Soggetti
Dermatology & Venereal Diseases",Surgery
Journal title
ISSN journal
10760512
Volume
21
Issue
10
Year of publication
1995
Pages
872 - 875
Database
ISI
SICI code
1076-0512(1995)21:10<872:TSOTCD>2.0.ZU;2-P
Abstract
BACKGROUND. The ''coup de fouet'' syndrome is an uncommon condition ch aracterized by a spontaneous intramuscular venous hemorrhage of the ca lf, sometimes accompanied by a deep thrombosis of the leg. OBJECTIVE. The purpose of this work is to verify the real incidence of the thromb otic complications, making use of the most recent noninvasive diagnost ic instruments, such as the duplex scanner and color Doppler. METHODS. From January 1992 to December 1993, we examined 24 subjects (average age, 38.5 years) suffering from the so-called ''coup de fouet'' syndro me, which had appeared during physical activity: walking (nine cases), running (six cases), and sudden changes of position (nine cases). In all cases we performed a clinical and instrumental examination (analog ical and tensive arterial and venous Doppler, arterial and venous dupl ex scanner, and color Doppler). RESULTS. Clinically we found, in 17 su bjects, a hematoma in the posterior calf with increased thickness and, in 10 cases, with spontaneous sharp pain. In the other seven cases we found a modest hematoma without subjective or other objective symptom s. The arterial Doppler and scanner findings were normal. In the first group of 17 cases, the average clinostatic Doppler venous pressure, m easured using a method developed by us and already described, was 32 /- 4 mm Hg (normal value, 15 +/- 7 mm Hg); in the other seven cases th e value was 19 +/- 4 mm Hg. CONCLUSION. The duplex scanner and color D oppler examination confirmed in all subjects the presence of an intraf ascial hematoma in the gemellar zone; in 10 cases (41.7%), with more p ainful symptomatology, in a zone contiguous to the hemorrhage, we foun d a gemellar (six cases) or popliteal (four cases) phlebothrombosis. L astly, we must point out that the syndrome is not always benign and th at, therefore, a correct and more vigilant diagnostic and therapeutic approach is necessary.