Langerhans cell histiocytosis of the orbit: A study of eight cases

BACKGROUND: Langerhans cell histiocytosis (LCH) of the orbit is a rare clinical entity with a diagnostic and therapeutic dilemma. MATERIALS AND METHODS: This was a retrospective study of eight patients with orbital LCH. RESULTS: All eight patients in our series were male, and the mean age at present...

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Main Authors: Swati Singh, Swathi Kaliki, Vijay Anandz Reddy Palkonda, Reddy Palkonda, Milind N Naik
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2018-01-01
Series:Oman Journal of Ophthalmology
Subjects:
eye
Online Access:http://www.ojoonline.org/article.asp?issn=0974-620X;year=2018;volume=11;issue=2;spage=134;epage=139;aulast=Singh
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spelling doaj-4d5d2fc788ae44598e4915cd77fdd6632020-11-24T22:18:13ZengWolters Kluwer Medknow PublicationsOman Journal of Ophthalmology0974-620X2018-01-0111213413910.4103/ojo.OJO_226_2016Langerhans cell histiocytosis of the orbit: A study of eight casesSwati SinghSwathi KalikiVijay Anandz Reddy PalkondaReddy PalkondaMilind N NaikBACKGROUND: Langerhans cell histiocytosis (LCH) of the orbit is a rare clinical entity with a diagnostic and therapeutic dilemma. MATERIALS AND METHODS: This was a retrospective study of eight patients with orbital LCH. RESULTS: All eight patients in our series were male, and the mean age at presentation was 8 years (median 6 years; range, 7 months–23 years). All of them had unilateral disease, and the most common presenting complaint was upper eyelid swelling (n = 6). The mean duration of symptoms was 6 weeks (median, 3 weeks; range, 2–20 weeks). Visual acuity was unaffected in seven cases. Clinical diagnosis included rhabdomyosarcoma (n = 4), malignant lacrimal gland tumor (n = 2), orbital cysticercosis (n = 1), and orbital tuberculosis (n = 1). The diagnosis of orbital LCH was confirmed by incisional biopsy (n = 7) or fine-needle aspiration cytology (n = 1). Four cases underwent careful limited curettage and received intralesional steroid, and four cases were treated with intralesional steroid alone after incisional biopsy. Complete tumor resolution was achieved in seven cases after receiving a mean of one intralesional steroid injection (median, 1; range, 1–2), while one patient was advised systemic chemotherapy for residual tumor. No tumor recurrence was noted in any case at a mean follow-up duration of 30 months (median, 23 months; range, 7–96 months). None of the cases developed diabetes insipidus or multisystem disease during the follow-up period. CONCLUSION: Minimal local intervention with intralesional steroids with/without careful curettage achieves complete tumor resolution in unifocal orbital LCH.http://www.ojoonline.org/article.asp?issn=0974-620X;year=2018;volume=11;issue=2;spage=134;epage=139;aulast=SinghEosinophilic granulomaeyeintralesional steroidsLangerhans cell histiocytosisorbit
collection DOAJ
language English
format Article
sources DOAJ
author Swati Singh
Swathi Kaliki
Vijay Anandz Reddy Palkonda
Reddy Palkonda
Milind N Naik
spellingShingle Swati Singh
Swathi Kaliki
Vijay Anandz Reddy Palkonda
Reddy Palkonda
Milind N Naik
Langerhans cell histiocytosis of the orbit: A study of eight cases
Oman Journal of Ophthalmology
Eosinophilic granuloma
eye
intralesional steroids
Langerhans cell histiocytosis
orbit
author_facet Swati Singh
Swathi Kaliki
Vijay Anandz Reddy Palkonda
Reddy Palkonda
Milind N Naik
author_sort Swati Singh
title Langerhans cell histiocytosis of the orbit: A study of eight cases
title_short Langerhans cell histiocytosis of the orbit: A study of eight cases
title_full Langerhans cell histiocytosis of the orbit: A study of eight cases
title_fullStr Langerhans cell histiocytosis of the orbit: A study of eight cases
title_full_unstemmed Langerhans cell histiocytosis of the orbit: A study of eight cases
title_sort langerhans cell histiocytosis of the orbit: a study of eight cases
publisher Wolters Kluwer Medknow Publications
series Oman Journal of Ophthalmology
issn 0974-620X
publishDate 2018-01-01
description BACKGROUND: Langerhans cell histiocytosis (LCH) of the orbit is a rare clinical entity with a diagnostic and therapeutic dilemma. MATERIALS AND METHODS: This was a retrospective study of eight patients with orbital LCH. RESULTS: All eight patients in our series were male, and the mean age at presentation was 8 years (median 6 years; range, 7 months–23 years). All of them had unilateral disease, and the most common presenting complaint was upper eyelid swelling (n = 6). The mean duration of symptoms was 6 weeks (median, 3 weeks; range, 2–20 weeks). Visual acuity was unaffected in seven cases. Clinical diagnosis included rhabdomyosarcoma (n = 4), malignant lacrimal gland tumor (n = 2), orbital cysticercosis (n = 1), and orbital tuberculosis (n = 1). The diagnosis of orbital LCH was confirmed by incisional biopsy (n = 7) or fine-needle aspiration cytology (n = 1). Four cases underwent careful limited curettage and received intralesional steroid, and four cases were treated with intralesional steroid alone after incisional biopsy. Complete tumor resolution was achieved in seven cases after receiving a mean of one intralesional steroid injection (median, 1; range, 1–2), while one patient was advised systemic chemotherapy for residual tumor. No tumor recurrence was noted in any case at a mean follow-up duration of 30 months (median, 23 months; range, 7–96 months). None of the cases developed diabetes insipidus or multisystem disease during the follow-up period. CONCLUSION: Minimal local intervention with intralesional steroids with/without careful curettage achieves complete tumor resolution in unifocal orbital LCH.
topic Eosinophilic granuloma
eye
intralesional steroids
Langerhans cell histiocytosis
orbit
url http://www.ojoonline.org/article.asp?issn=0974-620X;year=2018;volume=11;issue=2;spage=134;epage=139;aulast=Singh
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