Schick B, Kahle G, Kronsbein H, Draf W
Klinik für Hals-Nasen-Ohren-Krankheiten, Kopf-, Hals- und Plastische Gesichtschirurgie, Kommunikationsstörungen, Städtisches Klinikum Fulda.
HNO. 1996 Jun;44(6):329-32.
A papillary neoplasm that was presumed to originate from the endolymphatic sac was described by Heffner in 1989. This tumor was considered to be a "low-grade adenocarcinoma" because of its behavior: slow growth, local destruction and failure to metastasize. The clinical manifestations are hearing loss, vertigo, facial nerve paralysis and/or cerebellar disorders. Endolymphatic sac tumors have previously been mistaken for such neoplasms as paraganglioma, choroid plexus papilloma and carcinoma, adenomatous tumor of the middle ear and secondary metastases. The diagnosis of this neoplasm is facilitated by CT and MRI. The treatment of choice is total removal of tumor as soon as possible and requires clinical awareness of this rare but important pathologic entity.
1989年,赫夫纳描述了一种推测起源于内淋巴囊的乳头状肿瘤。由于其生长缓慢、局部破坏且不发生转移的特性,该肿瘤被认为是一种“低级别腺癌”。其临床表现为听力丧失、眩晕、面神经麻痹和/或小脑功能障碍。内淋巴囊肿瘤此前曾被误诊为副神经节瘤、脉络丛乳头状瘤和癌、中耳腺瘤性肿瘤以及继发性转移瘤等。CT和MRI有助于该肿瘤的诊断。首选治疗方法是尽快彻底切除肿瘤,这需要临床医生了解这种罕见但重要的病理实体。