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[Management of chicken pox purpura fulminans: a pediatric case report]
S Domergue1, M Rodiere, M Bigorre
1Service de chirurgie maxillofaciale et de chirurgie plastique infantile, hôpital Lapeyronie, avenue du doyen-Gaston-Giraud, 34000 Montpellier, France. domergue.sophie@caramail.com
Insights
A 4-year-old girl with chicken-pox purpura fulminans experienced rapid skin necrosis. Multidisciplinary management including anticoagulation and skin grafting led to a good long-term outcome.
Area of Science:
- Pediatrics
- Dermatology
- Hematology
Background:
- Purpura fulminans is a rare, severe thrombotic disorder often associated with infections.
- Chickenpox (varicella) can, in rare cases, trigger purpura fulminans, leading to extensive skin necrosis.
Observation:
- A 4-year-old girl presented with purpura fulminans 5 days after the onset of chickenpox.
- Lesions rapidly evolved into cutaneous and subcutaneous necrosis on her thighs and calf.
- Medical management included fresh plasma, blood, antithrombin III, fibrin, heparin, and activated protein C.
Findings:
- Surgical debridement of necrotic areas and subsequent skin grafting from the scalp were performed 5 weeks after presentation.
- The patient experienced rapid healing and good functional and aesthetic outcomes at a 3-year follow-up.
Implications:
- This case highlights the importance of a multidisciplinary approach in managing chicken-pox-associated purpura fulminans.
- Early medical intervention combined with delayed surgical management can lead to favorable outcomes.
- The scalp is a viable donor site for skin grafting in pediatric cases due to its abundant skin and minimal aesthetic impact.
Abstract:
The authors report a case of a 4 years old girl who had presented a chicken-pox purpura fulminans. Lesions appeared 5 days after chicken-pox start and were quickly evoluted in cutaneous and sub-cutaneous necrosis on external side of thighs and behind side of right calf. A medical management was done with fresh plasma, blood, antithrombine 3, and fibrin. Specifics treatments were done: heparin and activated C protein. Surgical treatment was realised 5 weeks later. It consisted of clean necrosis areas and put a thin skin graft witch was took on the scalp. The evolution was fast good. The follow-up is 3 years without big esthetic and functional consequences. Some cases of this pathology were described in literature with serious lesions. The management should be multidisciplinary. Surgical treatment should be realised when lesions are stabilized. Scalp is a donor site for skin graft very interesting because of big quantity of skin and not esthetic consequence.
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