CC BY-NC-ND 4.0 · J Neurol Surg Rep 2022; 83(03): e90-e94
DOI: 10.1055/a-1847-8245
Original Article

Resolution and Re-ossification of Orbital-Wall Langerhans Cell Histiocytosis Following Stereotactic Needle Biopsy

William C. Broaddus
1   Department of Neurosurgery, Virginia Commonwealth University, Richmond, Virginia, United States
,
Aravind Somasundaram
1   Department of Neurosurgery, Virginia Commonwealth University, Richmond, Virginia, United States
,
1   Department of Neurosurgery, Virginia Commonwealth University, Richmond, Virginia, United States
,
Charles F. Opalak
1   Department of Neurosurgery, Virginia Commonwealth University, Richmond, Virginia, United States
,
Hope T. Richard
2   Department of Pathology, Virginia Commonwealth University, Richmond, Virginia, United States
,
Sharon B. Wolber
1   Department of Neurosurgery, Virginia Commonwealth University, Richmond, Virginia, United States
,
Hayri E. Sangiray
1   Department of Neurosurgery, Virginia Commonwealth University, Richmond, Virginia, United States
› Author Affiliations
Funding None.

Abstract

Introduction Langerhans cell histiocytosis (LCH) is a rare disease that encompasses a spectrum of clinical syndromes. It is characterized by the proliferation and infiltration of white blood cells into organs or organ systems. Reports of management of these lesions have included biopsy, resection, curettage, radiation, and/or chemotherapy.

Case Presentation A 40-year-old man presented with a history of right proptosis and retro-orbital pain and was found to have a lytic mass involving the greater wing of the sphenoid extending into the right orbit. A stereotactic needle biopsy using neuronavigation demonstrated this to be LCH. After no further treatment, the mass spontaneously resolved, with virtual normalization of the orbital magnetic resonance imaging at 10 months following the needle biopsy. The bony defect of the temporal bone caused by the mass also re-ossified following the needle biopsy.

Discussion This report highlights the potential for an isolated LCH lesion to regress after simple needle biopsy, an outcome only rarely reported previously. Thus, expectant management of such lesions following biopsy or initial debridement should be considered prior to proceeding with additional treatment.



Publication History

Received: 09 June 2021

Accepted: 29 March 2022

Accepted Manuscript online:
10 May 2022

Article published online:
19 July 2022

© 2022. The Author(s). This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commercial purposes, or adapted, remixed, transformed or built upon. (https://creativecommons.org/licenses/by-nc-nd/4.0/)

Georg Thieme Verlag KG
Rüdigerstraße 14, 70469 Stuttgart, Germany

 
  • References

  • 1 Hand A. Polyuria and tuberculosis. Arch Pediatr 1893; 10: 673-675
  • 2 Donadieu J, Chalard F, Jeziorski E. Medical management of langerhans cell histiocytosis from diagnosis to treatment. Expert Opin Pharmacother 2012; 13 (09) 1309-1322
  • 3 Rajendram R, Rose G, Luthert P, Plowman P, Pearson A. Biopsy-confirmed spontaneous resolution of orbital langerhans cell histiocytosis. Orbit 2005; 24 (01) 39-41
  • 4 Lee SK, Jung TY, Jung S, Han DK, Lee JK, Baek HJ. Solitary Langerhans cell histocytosis of skull and spine in pediatric and adult patients. Childs Nerv Syst 2014; 30 (02) 271-275
  • 5 DiCaprio MR, Roberts TT. Diagnosis and management of langerhans cell histiocytosis. J Am Acad Orthop Surg 2014; 22 (10) 643-652
  • 6 Giovannetti F, Giona F, Ungari C. et al. Langerhans cell histiocytosis with orbital involvement: our experience. J Oral Maxillofac Surg 2009; 67 (01) 212-216
  • 7 Harris GJ, Woo KI. Eosinophilic granuloma of the orbit: a paradox of aggressive destruction responsive to minimal intervention. Trans Am Ophthalmol Soc 2003; 101: 93-103 , discussion 103–105
  • 8 Garrity JA, Henderson JW, Cameron JD. Henderson's Orbital Tumors. Philadelphia, PA: Lippincott Williams & Wilkins; 2007. :267
  • 9 Kiratli H, Tarlan B, Söylemezoglu F. Langerhans cell histiocytosis of the orbit. Eur J Ophthalmol 2013; 23 (04) 578-583
  • 10 Shields JA, Shields CL, Scartozzi R. Survey of 1264 patients with orbital tumors and simulating lesions: The 2002 Montgomery Lecture, part 1. Ophthalmology 2004; 111 (05) 997-1008
  • 11 Glover AT, Grove Jr AS. Eosinophilic granuloma of the orbit with spontaneous healing. Ophthalmology 1987; 94 (08) 1008-1012
  • 12 El Ayadi C, Benharbit M, Lezrek M, Tachfouti S, Boutimzine N, Daoudi R. Solitary eosinophilic granuloma of the orbit: a case report [in French]. Bull Soc Belge Ophtalmol 2007; (305) 33-36
  • 13 Harzallah L, Braham N, Ben Chérifa L. et al. Solitary eosinophilic granuloma of the orbit: a case report [in French]. J Fr Ophtalmol 2005; 28 (09) 983
  • 14 Smith JH, Fulton L, O'Brien JM. Spontaneous regression of orbital Langerhans cell granulomatosis in a three-year-old girl. Am J Ophthalmol 1999; 128 (01) 119-121
  • 15 Satoh K, Tada M, Shimizu H, Yoneoka Y. Early adult-onset orbital apex Langerhans cell histiocytosis histologically confirmed during “truly spontaneous” regression. Acta Neurochir (Wien) 2012; 154 (02) 301-302
  • 16 Abla O, Egeler RM, Weitzman S. Langerhans cell histiocytosis: current concepts and treatments. Cancer Treat Rev 2010; 36 (04) 354-359
  • 17 Wladis EJ, Tomaszewski JE, Gausas RE. Langerhans cell histiocytosis of the orbit 10 years after involvement at other sites. Ophthal Plast Reconstr Surg 2008; 24 (02) 142-143