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1.
J Neurosurg Pediatr ; 27(2): 151-159, 2020 Dec 04.
Artigo em Inglês | MEDLINE | ID: mdl-33276328

RESUMO

Split notochord syndrome (SNS) is a rare congenital defect of the central nervous system and has been associated with several anomalies affecting multiple organ systems. One association has been communication with the gastrointestinal tract and the spine, previously identified as a neuroenteric fistula (NEF). Here, the authors describe the unique case of a female infant with SNS and NEF treated with a multistage surgical repair. The three-stage operative plan included a two-stage repair of the defect and temporary subgaleal shunting followed by delayed ventriculoperitoneal shunt placement. The infant recovered well postsurgery and over a 5-year follow-up. A case description, surgical techniques, and rationale are reported. Additionally, a systematic review of the literature utilizing the MEDLINE database was performed.Treatment of SNS with NEF using a multidisciplinary multistaged approach to repair the intestinal defect, close the neural elements, and divert cerebrospinal fluid to the peritoneum is shown to be a safe and viable option for future cases.


Assuntos
Fístula/cirurgia , Trato Gastrointestinal/cirurgia , Procedimentos Neurocirúrgicos/métodos , Notocorda/anormalidades , Notocorda/cirurgia , Doenças da Medula Espinal/cirurgia , Feminino , Humanos , Recém-Nascido , Espinha Bífida Cística/complicações , Espinha Bífida Cística/cirurgia , Disrafismo Espinal/complicações , Disrafismo Espinal/cirurgia , Síndrome , Resultado do Tratamento , Derivação Ventriculoperitoneal
2.
J La State Med Soc ; 161(1): 41-4, 2009.
Artigo em Inglês | MEDLINE | ID: mdl-19278169

RESUMO

BACKGROUND: Undifferentiated (embryonal) sarcoma (UES) of the liver is a malignant hepatic neoplasm accounting for 7% of pediatric hepatic tumors. Current use of multimodal therapy, including chemotherapy and surgery, has greatly improved survival. Tumor rupture is uncommon and, prior to the adjuvant use of sarcoma based chemotherapy regimens, was thought to be poor prognostic sign. CASE PRESENTATION AND DISCUSSION: A 10-year-old girl presented with acute worsening of abdominal pain while being worked up for liver mass. At surgery, she was found to have a ruptured, 20 x 15 x 5 centimeter (cm) UES, the largest reported ruptured UES to be resected primarily. The size and position of her tumor required very aggressive surgery for complete resection. She subsequently received adjuvant chemotherapy and radiation. Twenty-four months following surgery she is doing well with no evidence of disease. CONCLUSION: Despite tumor rupture, complete tumor resection gives the patient the best chance of long-term survival. Aggressive surgery is warranted if the tumor can be completely resected.


Assuntos
Neoplasias Embrionárias de Células Germinativas/cirurgia , Sarcoma/cirurgia , Diferenciação Celular , Criança , Feminino , Humanos , Neoplasias Embrionárias de Células Germinativas/diagnóstico por imagem , Neoplasias Embrionárias de Células Germinativas/patologia , Radiografia , Literatura de Revisão como Assunto , Sarcoma/patologia
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