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1.
Pediatr Surg Int ; 40(1): 64, 2024 Mar 03.
Artículo en Inglés | MEDLINE | ID: mdl-38433161

RESUMEN

The aim of this study is to review the indications of pedicled flaps and analyze the results. A observational retrospective study of under 18-year-old oncology patients who required reconstructive surgery with pedicled flaps between 2011 and 2022 was performed. Demographic and clinical variables, indications, complications, and outcomes were collected. 236 patients were reviewed and 13 met inclusion criteria, eight girls and five boys (mean age: 10.6 years). Indications were Ewing's sarcoma (5), osteosarcoma (5), neuroblastoma, desmoid tumor, and neurofibroma. Preoperative PET-CT, MRI and bone scintigraphy were performed. The flaps were used on costal and extremity reconstruction: latissimus dorsi (5), pectoralis (2), medial gastrocnemius (2), combined latissimus dorsi, trapezius and serratus muscle, biceps femoris, fascio-neuro-cutaneous saphenous and cutaneous advancement-rotation. Two were performed on allograft and eight on prosthesis. All allowed immediate and complete closure. Six patients received intraoperative radiotherapy. One flap infection and two vascular complications were reported, a total necrosis, which required a new flap, and a partial necrosis, treated with a local plasty. Chemotherapy was resumed after 21 days (15-31). Mean follow-up time was 5.34 years. Flaps are an effective therapeutic option allowing reconstruction of large defects after pediatric oncologic surgeries. The most frequent complication was vascular.


Asunto(s)
Tomografía Computarizada por Tomografía de Emisión de Positrones , Colgajos Quirúrgicos , Masculino , Femenino , Humanos , Niño , Adolescente , Estudios Retrospectivos , Extremidades , Necrosis
2.
Pediatr Infect Dis J ; 40(10): e384-e387, 2021 10 01.
Artículo en Inglés | MEDLINE | ID: mdl-34292272

RESUMEN

Fournier's gangrene is a necrotizing fasciitis of the scrotal and inguinal region, associating high mortality and complication rates. It is extremely rare in the neonatal period and may be life threatening. We present an exceptional case of a 24-day-old boy who consulted to the emergency department for fever (39 °C) and an indurated, fluctuating and painful erythema in both groins, left hemiscrotum, left anterior femoral region and perineum for the last 6 hours. Blood analysis showed increased acute phase reactants without leukocytosis. Ultrasound revealed significant soft-tissue involvement. Due to high clinical suspicion and hemodynamic instability (tachycardia and prolonged capillary filling), urgent fasciotomy, placement of Penrose drains and intensive irrigation was performed. Wound care with irrigations was performed 3 times a day. During the 12 days neonatal intensive care unit admission, he required hemodynamic support and orotracheal intubation and sedation for pain control. Broad-spectrum antibiotic therapy (with cefotaxime, clindamycin and cloxacillin) was administered for 2 weeks. Ampicillin-sensitive Streptococcus pyogenes (Group A) was isolated in blood culture at 4th day of admission allowing antibiotic de-escalation. He was discharged on postoperative day 24. He has minimal, inconspicuous scars and no functional sequelae. Fever in neonates requires close observation considering the use of empirical broad-spectrum antibiotics and hospitalization. Early diagnosis, prompt surgical management and broad-spectrum antibiotic therapy are essential to prevent complication. Early fasciotomy with intensive irrigation and close survey may avoid extensive skin debridement.


Asunto(s)
Desbridamiento/métodos , Gangrena de Fournier/diagnóstico por imagen , Antibacterianos/uso terapéutico , Fascitis Necrotizante/diagnóstico por imagen , Fascitis Necrotizante/tratamiento farmacológico , Fascitis Necrotizante/cirugía , Gangrena de Fournier/tratamiento farmacológico , Gangrena de Fournier/cirugía , Hospitalización , Humanos , Recién Nacido , Masculino , Escroto/diagnóstico por imagen , Escroto/patología , Resultado del Tratamiento , Ultrasonografía
4.
Pediatr Dermatol ; 36(5): 745-746, 2019 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-31355485

RESUMEN

Midline dermoid cysts are uncommon lesions that can lead to severe complications when an intracranial extension exists. We report the cases of two twin sisters referred to surgery for removal of the masses and the intracranial extension. They represent an additional example of familial nasal dermoid cysts, providing further support for a genetic basis for the disorder.


Asunto(s)
Quiste Dermoide/congénito , Enfermedades en Gemelos/congénito , Neoplasias Nasales/congénito , Neoplasias Cutáneas/congénito , Gemelos Monocigóticos , Quiste Dermoide/patología , Enfermedades en Gemelos/patología , Femenino , Humanos , Lactante , Neoplasias Nasales/patología , Neoplasias Cutáneas/patología
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