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Eosinophilic Granuloma: A Rare and Often Benign Condition Presenting as a Lump on the Head, which was Easily Treated.嗜酸性肉芽肿：一种罕见且通常为良性的病症，表现为头部肿块，易于治疗。
Eur J Case Rep Intern Med. 2021 Jul 20;8(7):002727. doi: 10.12890/2021_002727. eCollection 2021.
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本文引用的文献

1
Langerhans cell histiocytosis of the shoulder girdle, pelvis and extremities: a review of radiographic and MRI features in 85 cases.肩带、骨盆和四肢的朗格汉斯细胞组织细胞增生症：85 例的影像学和 MRI 特征回顾。
Skeletal Radiol. 2020 Dec;49(12):1925-1937. doi: 10.1007/s00256-020-03472-2. Epub 2020 May 26.
2
Direct injection of methylprednisolone sodium succinate in the treatment of solitary eosinophilic granuloma of bone: a report of 9 cases.直接注射琥珀酸甲泼尼龙治疗骨孤立性嗜酸性肉芽肿：9例报告
Radiology. 1980 Aug;136(2):289-93. doi: 10.1148/radiology.136.2.7403498.

嗜酸性肉芽肿：一种罕见且通常为良性的病症，表现为头部肿块，易于治疗。

Eosinophilic Granuloma: A Rare and Often Benign Condition Presenting as a Lump on the Head, which was Easily Treated.

作者信息

Pires Tatiana, Duarte Santos Catarina, Gonzalez Santos Miguel, Luz Luis, Ferrão Ana, Banza Maria J

机构信息

Department of Internal Medicine, Centro Hospitalar de Leiria, Leiria, Portugal.

出版信息

Eur J Case Rep Intern Med. 2021 Jul 20;8(7):002727. doi: 10.12890/2021_002727. eCollection 2021.

DOI:10.12890/2021_002727
PMID:34377705
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8336745/
Abstract

UNLABELLED

Eosinophilic granuloma is a localized, non-invasive form of Langerhans cell histiocytosis. It usually develops in the long bones and is more frequent in children under the age of 10 years. It is very rare in adults. We present the case of a young woman admitted to hospital for persistent refractory left parietal headache, later revealed to be caused by an eosinophilic granuloma.

LEARNING POINTS

Eosinophilic granuloma is a localized benign form of Langerhans cell histiocytosis.It is essential to exclude the presence of bone lesions in other locations and/or systemic involvement.The prognosis is good, with surgical resection, when necessary, being a curative intervention, although sometimes (as in this case) a conservative approach is sufficient.

摘要

未标注

嗜酸性肉芽肿是朗格汉斯细胞组织细胞增多症的一种局限性、非侵袭性形式。它通常发生于长骨，在10岁以下儿童中更为常见。在成人中非常罕见。我们报告一例年轻女性因持续性难治性左侧顶叶头痛入院，后来发现是由嗜酸性肉芽肿引起的。

学习要点

嗜酸性肉芽肿是朗格汉斯细胞组织细胞增多症的一种局限性良性形式。排除其他部位骨病变和/或全身受累的情况至关重要。预后良好，必要时手术切除是一种治愈性干预措施，尽管有时（如本例）保守治疗就足够了。