累及颞骨的朗格汉斯细胞组织细胞增生症,伴有骨性迷宫边界的破坏和随后的再化生。

IF 1.3 4区 医学 Q3 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Rofo-fortschritte Auf Dem Gebiet Der Rontgenstrahlen Und Der Bildgebenden Verfahren Pub Date : 2024-10-01 Epub Date: 2024-02-19 DOI:10.1055/a-2254-5536
Katja Döring, Philipp Ivanyi, Heinrich Lanfermann, Athanasia Warnecke, Anja Giesemann
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引用次数: 0

摘要

目的:朗格汉斯细胞组织细胞增生症(Langerhans cell histiocytosis,LCH)每年的发病率在 1-9/10 万之间,是血液肿瘤疾病谱中一种相当罕见的疾病(Hayes 等,2009 年)。这种组织细胞增生的肿瘤性疾病可表现为局部器官或浸润多个器官的播散性疾病。其中约 25-30% 的病例表现为颞骨受累(Ni 等人,2017 年):一名 41 岁女性因持续三年的眩晕、慢性乳突炎和急性进行性双侧听力下降(r > l)三周到急诊科就诊。深静脉血栓显示两侧颞骨的大部分都有广泛的骨质破坏,涉及前庭器官、耳蜗和内耳道。为了证实系统性炎症过程的怀疑,对乳突进行了PE检查,并通过活检确认为LCH。随后开始了全身治疗。治疗后的影像学检查显示,患者的病情几乎完全缓解,原有的缺损区重新变小,内耳道和迷宫结构再次出现骨性边缘。临床上,患者的植物神经症状有所改善,但仍存在双侧感音神经性听力损失:讨论:颞骨 LCH 是一种罕见的疾病,由于其临床表现无特异性,常常被误诊。认识颞骨 LCH 及其在成人中的发生对于准确和一致的诊断至关重要:- 要点:LCH 是一种相当罕见的血液肿瘤疾病。- 颞骨受累,尤其是如此广泛的颞骨受累(如本病例报告中的情况),在成年期是相当不典型的。- 采用系统治疗后,病情得到缓解。- 治疗后骨质结构完全恢复。- 植入的人工耳蜗可以弥补听力损失。
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Langerhans cell histiocytosis involving the temporal bone with destruction and subsequent reossification of the bony labyrinth boundaries.

Purpose:  With an incidence between 1-9/100 000 per year, Langerhans cell histiocytosis (LCH) is a rather rare disease from the hemato-oncologic disease spectrum (Hayes et al. 2009). The tumorlike disease with proliferation of histiocytic cells may manifest as localized to one organ or disseminated with infiltration of a wide variety of organs. Approximately 25-30 % of these cases show involvement of the temporal bone (Ni et al. 2017).

Case description:  With vertigo persisting for three years, chronic mastoiditis, and acute progressive hearing loss bilaterally (r > l) for three weeks, a 41-year-old woman presented at an emergency department. The DVT showed extensive bony destruction of large parts of the temporal bone on both sides, involving the vestibular organ, the cochlea, and the internal auditory canal. To confirm the suspicion of a systemic inflammatory process, a PE was performed from the mastoid with bioptic confirmation of an LCH. Systemic therapy was initiated. Post-therapeutic imaging showed almost complete remission with reossification of the preexisting defect zones and the internal auditory canal and labyrinth structures again showed bony margins. Clinically, there was an improvement of the vegetative symptoms with remaining bilateral sensorineural hearing loss.

Discussion:  LCH of the temporal bone is a rare and often misdiagnosed disease due to its nonspecific clinical presentation. Awareness of temporal bone LCH and its occurrence in adults is essential for accurate and consistent diagnosis.

Key points:   · LCH is a rather rare disease from the hemato-oncological spectrum. · Affection of the temporal bone, especially such an extensive one (as in this case report), is rather atypical in adulthood. · Use of systemic therapy resulted in remission. · There was complete reossification of the osseous structures post-therapy. · A cochlear implant was able to be implanted to compensate for hearing loss.

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