眼眶朗格汉斯细胞组织细胞增多症活检后自发性消退1例报告。眼眶朗格汉斯细胞组织细胞增多症的自发消退。

IF 0.9 Q4 ONCOLOGY
Rare Tumors Pub Date : 2022-10-18 eCollection Date: 2022-01-01 DOI:10.1177/20363613221135987
Safia Yahiaoui, Asma Ghorbel, Khadija Ben Zid, Semia Zarraa, Lina Kchaou, FidaNoubigh, Wael Kaabia, Fadoua Bouguerra, Alia Mousli, Rim Abidi, Amani Yousfi, Boujelbene Nadia, Chiraz Nasr
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引用次数: 0

摘要

朗格汉斯组织细胞增生症(LCH)是一种罕见的良性病理,占眼眶肿瘤的不到1%。它可以引起局部或全身性病变,导致硬组织和软组织的破坏。嗜酸性肉芽肿是LCH最良性的形式和主要的临床表现。我们报告一个18岁男性患者眼眶受累的嗜酸性肉芽肿病例。最初计划眼眶放射治疗,但最终因切口活检后病变自发消退而未进行。鉴于活检后自发消退的可能性,特别是在小病变中,所提出的病例支持期待的态度。然而,考虑到复发的风险,长期随访是必要的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Spontaneous regression of an orbital Langerhans cell histiocytosis after biopsy: A case report. Spontaneous regression of an orbital Langerhans cell histiocytosis.

Spontaneous regression of an orbital Langerhans cell histiocytosis after biopsy: A case report. Spontaneous regression of an orbital Langerhans cell histiocytosis.

Spontaneous regression of an orbital Langerhans cell histiocytosis after biopsy: A case report. Spontaneous regression of an orbital Langerhans cell histiocytosis.

Spontaneous regression of an orbital Langerhans cell histiocytosis after biopsy: A case report. Spontaneous regression of an orbital Langerhans cell histiocytosis.

Langerhans histiocytosis or Langerhans cell histiocytosis (LCH) is a rare benign pathology representing less than 1% of orbital tumors. It can cause either localized or generalized lesions, leading to the destruction of hard and soft tissues. Eosinophilic granuloma is the most benign form and the predominant clinical presentation of LCH. We report a case of eosinophilic granuloma with orbital involvement in an 18-year-old male patient. Orbital radiotherapy was initially planned, but finally it was not performed due to a spontaneous regression of the lesion after the incisional biopsy. The presented case supports an expectant attitude given the possibility of a spontaneous regression after the biopsy, especially in small lesions. However, long-term follow-up is essential given the risk of recurrence.

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Rare Tumors
Rare Tumors ONCOLOGY-
CiteScore
1.50
自引率
0.00%
发文量
15
审稿时长
15 weeks
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