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Radiotherapy for Langerhans cell histiocytosis with paraplegia: A rare oncologic emergency case report in infancy and literature review.
Nakashima, Kentaro; Koga, Yuhki; Sakai, Yasunari; Takada, Hidetoshi; Harimaya, Katsumi; Ohga, Saiji; Taguchi, Tomoaki; Oda, Yoshinao; Honda, Hiroshi; Ohga, Shouichi.
Afiliación
  • Nakashima K; Department of Pediatrics, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.
  • Koga Y; Department of Pediatrics, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.
  • Sakai Y; Department of Pediatrics, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan. Electronic address: ysakai22q13@gmail.com.
  • Takada H; Department of Pediatrics, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan; Department of Perinatal and Pediatric Medicine, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.
  • Harimaya K; Department of Orthopedic Surgery, Kyushu University, Fukuoka, Japan.
  • Ohga S; Department of Radiology, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.
  • Taguchi T; Department of Pediatric Surgery, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.
  • Oda Y; Department of Pathology, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.
  • Honda H; Department of Radiology, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.
  • Ohga S; Department of Pediatrics, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.
Brain Dev ; 40(10): 952-955, 2018 Nov.
Article en En | MEDLINE | ID: mdl-29907475
ABSTRACT

BACKGROUND:

Langerhans cell histiocytosis (LCH) is a clonal disease with focal or disseminated lesions that may compress the surrounding tissues, including the spinal cord. Because few reports have described the spinal symptoms as the first manifestation of pediatric LCH, the long-term neurological outcomes remain unclear. CASE REPORT AND LITERATURE REVIEW We report a 21-month-old boy who presented with sudden-onset paraplegia. Imaging analyses revealed that osteolytic lesions and epidural tumors compressing the spinal cord at the T7-9 vertebrae. Twelve days after he developed leg weakness, emergency radiotherapy was started after a tumor biopsy. During the course of radiotherapy, paralysis steadily ameliorated. After we excluded infections and determined the pathological diagnosis of LCH, multi-drug chemotherapy was started. Apparent improvement in his complete paraplegia was observed after a total 15 Gy of radiotherapy and subsequent chemotherapy, leaving no neurological sequelae at 4 years of age. Through a literature search of studies published from 1980 to 2017, we found that children with LCH showed a generally favorable recovery from neurological dysfunction after the acute phase of spinal symptoms.

CONCLUSION:

This report underscores the utility of emergency radiotherapy for the neurological recovery of spinal LCH in infants. Our long-term observation further denotes the value of this treatment in terms of the intact survival with preserved motor functions and physical growth.
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Texto completo: 1 Colección: 01-internacional Asunto principal: Neoplasias Epidurales / Histiocitosis de Células de Langerhans Tipo de estudio: Etiology_studies Límite: Humans / Infant / Male Idioma: En Revista: Brain Dev Año: 2018 Tipo del documento: Article País de afiliación: Japón

Texto completo: 1 Colección: 01-internacional Asunto principal: Neoplasias Epidurales / Histiocitosis de Células de Langerhans Tipo de estudio: Etiology_studies Límite: Humans / Infant / Male Idioma: En Revista: Brain Dev Año: 2018 Tipo del documento: Article País de afiliación: Japón