Literature DB >> 11549922

Occipital aneurysmal bone cyst secondary to eosinophilic granuloma.

F Roncaroli1, A Consales, E Galassi, B Bernardi, B Valeri.   

Abstract

We describe the case of a 2-year-old male patient with an aneurysmal bone cyst (ABC) of the occiput secondary to unifocal eosinophilic granuloma (EG). The lesion presented as a painless mass of the scalp which had grown rapidly over the 2 weeks prior to admission. Radiologically, the lesion was osteolytic and multicystic with fluid-fluid levels. On histology, the cyst wall contained hemosiderin-laden histiocytes, spindle cells, multinucleated giant cells, Langerhans' cells and eosinophils. Surgical treatment consisted of en bloc resection. Fourteen months after surgery, the patient was well with no local recurrence. Association between EG and ABC is rare. To our knowledge, this is the first case involving the skull. Copyright 2001 S. Karger AG, Basel

Entities:  

Mesh:

Year:  2001        PMID: 11549922     DOI: 10.1159/000050399

Source DB:  PubMed          Journal:  Pediatr Neurosurg        ISSN: 1016-2291            Impact factor:   1.162


  3 in total

1.  Fluid-fluid levels in transcalvarial Langerhans' cell histiocytosis.

Authors:  Ajay Taranath; Ella Onikul
Journal:  Pediatr Radiol       Date:  2004-01-28

2.  CT and MRI of pediatric skull lesions with fluid-fluid levels.

Authors:  S A Nabavizadeh; L T Bilaniuk; T Feygin; K V Shekdar; R A Zimmerman; A Vossough
Journal:  AJNR Am J Neuroradiol       Date:  2013-08-22       Impact factor: 3.825

3.  Clinical and magnetic resonance imaging feature differences between solitary and multiple type Langerhans cell histiocytosis involving the craniofacial bone.

Authors:  Shu Matsushita; Taro Shimono; Tomohisa Okuma; Takeshi Inoue; Takao Manabe; Yukio Miki
Journal:  Heliyon       Date:  2022-01-11
  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.