Literature DB >> 21667741

Vertebral Langerhans cell histiocytosis in an adult patient: case report and review of the literature.

George Sapkas1, Michael Papadakis.   

Abstract

Vertebral Langerhans cell histiocytosis, formerly called Histiocytosis X, is rarely seen in adults: a systematic non-quantitative review of the literature yielded only 27 cases. Vertebra plana is often associated in children, but this is not a feature in the adult population. The authors report the case of a 29-year-old woman with a two-month history of lumbar pain. Osteolysis of the right pedicle of L2 was noted on CT and MRI. Transpedicular curettage and fusion L1L3 were performed. Histopathological examination revealed Langerhans cell histiocytosis. Although rare, Langerhans cell histiocytosis should be included in the differential diagnosis of the solitary lytic vertebral lesion in the adult. Good results have been reported, in the absence of systemic manifestations, with the most conservative approach possible.

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Year:  2011        PMID: 21667741

Source DB:  PubMed          Journal:  Acta Orthop Belg        ISSN: 0001-6462            Impact factor:   0.500


  2 in total

1.  Langerhans cell histiocytosis of atlantoaxial joint in a middle-aged man presenting with deafness as first symptom and soft-tissue mass at neck showing excellent response to radiotherapy alone: Report of an extremely rare and unusual clinical condition and review of literature.

Authors:  Dodul Mondal; P K Julka; Manisha Jana; Ritika Walia; Tamojit Chaudhuri
Journal:  Ann Indian Acad Neurol       Date:  2014-10       Impact factor: 1.383

2.  Evaluation of pituitary uptake incidentally identified on 18F-FDG PET/CT scan.

Authors:  Huijun Ju; Jinxin Zhou; Yu Pan; Jing Lv; Yifan Zhang
Journal:  Oncotarget       Date:  2017-02-16
  2 in total

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