Literature DB >> 21570265

[Orbital location of multivisceral Langerhans-cell histiocytosis].

M Abdellaoui1, A-I Benatiya, S Bhallil, H Tahri.   

Abstract

Langerhans-cell histiocytosis is a rare disease accounting for less than 1% of orbital tumours. We report the case of an 18-month-old infant presenting with exophthalmos of the left eye lasting for 3 months in a context of deterioration of the general condition, polydipsia, and polyuria. The computed tomographic scan revealed an orbital cellular mass with a lytic bone lesion within the orbital roof and infiltration of frontopalpebral soft tissue. In addition, other secondary lesions were found at the skull, ribs, skin, liver, and spleen. The cytological study after biopsy showed infiltrates of histiocytes derived from Langerhans cells. Because the disease was multivisceral, the child was treated with chemotherapy (vinblastine) combined with a steroid and progressed well. At 30 months of follow-up, there was no evidence of recurrence or systemic involvement.
Copyright © 2011. Published by Elsevier SAS.

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Year:  2011        PMID: 21570265     DOI: 10.1016/j.arcped.2011.03.018

Source DB:  PubMed          Journal:  Arch Pediatr        ISSN: 0929-693X            Impact factor:   1.180


  1 in total

1.  Insufficiency of bone scintigraphy in vertebral lesions of langerhans cell histiocytosis compared to f-18 fluorodeoxyglucose positron emission tomography/computed tomography and diagnostic computed tomography.

Authors:  Zehra Pınar Koç; Selçuk Şimşek; Saadet Akarsu; Tansel Ansal Balcı; Mehmet Ruhi Onur; Ferat Kepenek
Journal:  Mol Imaging Radionucl Ther       Date:  2015-02-05
  1 in total

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