Modest Mara C, Garcia Joaquin J, Arndt Carola S, Carlson Matthew L
Department of Otolaryngology-Head and Neck Surgery, Mayo Clinic School of Medicine, Rochester, Minnesota, U.S.A.
Department of Pathology, Mayo Clinic School of Medicine, Rochester, Minnesota, U.S.A.
Laryngoscope. 2016 Aug;126(8):1899-904. doi: 10.1002/lary.25773. Epub 2015 Nov 4.
OBJECTIVES/HYPOTHESIS: Evaluate presentation, management, and clinical outcomes of patients with temporal bone Langerhans cell histiocytosis (LCH).
Retrospective chart review.
Reviewed all patients with temporal bone LCH at a tertiary academic referral center between 1978 and 2014. Presentation, disease course, intervention, and clinical outcomes were analyzed.
Between 1978 and 2014, 29 temporal bones in 20 patients (12 males; median age 32 years, range 1.3-88 years) were diagnosed with temporal bone LCH, representing 4% of all patients diagnosed with LCH at our institution during that time. Twelve (60%) patients presented purely with head and neck disease, nine (45%) with bilateral temporal bone involvement, seven (35%) with intracranial spread, and eight (40%) with multisystem disease. The most common presenting symptoms were otorrhea (n = 11; 55%) and subjective hearing loss (n = 10; 50%). Treatment included primary chemotherapy or radiation alone(n = 7; 35%), local resection alone (n = 2; 10%), and chemotherapy or radiation with surgery(n = 11; 55%). Ten patients suffered local or systemic relapse (50%; median 12 months). Median follow-up for patients was 31 months. One patient died secondary to pulmonary complications of multisystem LCH.
LCH is an uncommon histiocytic disorder with a range of clinical manifestations and disease severity. Otologic involvement is rare, and frequently manifests with symptoms similar to otomastoiditis. Evaluation and close follow-up of both ears is important. Bilateral simultaneous or sequential LCH can be seen in up to 45% of cases. Patients with temporal bone LCH should be managed by a multidisciplinary team with treatment tailored to the patient. Relapse is more common in patients with multisystem involvement. Even in subjects with isolated otologic involvement, long-term follow-up is critical, with relapses occurring years beyond treatment.
目的/假设:评估颞骨朗格汉斯细胞组织细胞增多症(LCH)患者的临床表现、治疗及临床结局。
回顾性病历审查。
对1978年至2014年间在一家三级学术转诊中心诊断为颞骨LCH的所有患者进行回顾。分析其临床表现、病程、干预措施及临床结局。
1978年至2014年间,20例患者(12例男性;中位年龄32岁,范围1.3 - 88岁)的29块颞骨被诊断为颞骨LCH,占该时期我院所有诊断为LCH患者的4%。12例(60%)患者仅表现为头颈部疾病,9例(45%)双侧颞骨受累,7例(35%)有颅内扩散,8例(40%)有多系统疾病。最常见的临床表现为耳漏(n = 11;55%)和主观听力下降(n = 10;50%)。治疗包括单纯初始化疗或放疗(n = 7;35%)、单纯局部切除(n = 2;10%)以及化疗或放疗联合手术(n = 11;55%)。10例患者出现局部或全身复发(50%;中位时间12个月)。患者的中位随访时间为31个月。1例患者死于多系统LCH的肺部并发症。
LCH是一种罕见的组织细胞疾病,具有一系列临床表现和疾病严重程度。耳部受累罕见,且常表现出与中耳乳突炎相似的症状。双耳评估及密切随访很重要。高达45%的病例可出现双侧同时或先后发生的LCH。颞骨LCH患者应由多学科团队管理,治疗应根据患者情况量身定制。多系统受累患者复发更常见。即使是孤立耳部受累的患者,长期随访也至关重要,复发可能在治疗多年后发生。
4。《喉镜》,126:1899 - 1904,2016年。