Delisle M B, Uro E, Rouquette I, Yardeni E, Rumeau J L
Department of Pathology, Rangueil University Hospital, Toulouse, France.
J Clin Pathol. 1994 Oct;47(10):959-61. doi: 10.1136/jcp.47.10.959.
Glandular tumours involving the middle ear and the mastoid are rare, and distinguishing between adenoma and adenocarcinoma is difficult. Two distinct histopathological patterns are accepted. While their clinical presentation differs, both require primary surgical treatment and both have a high rate of local recurrence. The papillary form takes a more aggressive course and wider regional spread. This pattern occurs predominantly in women. Its microscopic appearance and clinical course have been extensively described by Heffner who considered it as "low-grade adenocarcinoma of probable endolymphatic sac origin". A few cases have been associated with von Hippel-Lindau disease. The case of a 32 year old black woman is described. It is suggested that papillary adenocarcinoma of the endolymphatic sac should be considered in the spectrum of neoplasms seen in von Hippel-Lindau disease.
累及中耳和乳突的腺性肿瘤较为罕见,鉴别腺瘤和腺癌也很困难。目前认可两种不同的组织病理学模式。虽然它们的临床表现有所不同,但都需要进行初次手术治疗,且局部复发率都很高。乳头状形态的病程更为侵袭性,区域扩散范围更广。这种模式主要发生在女性中。其微观表现和临床病程已被赫夫纳广泛描述,他将其视为“可能起源于内淋巴囊的低级别腺癌”。少数病例与冯·希佩尔-林道病有关。本文描述了一名32岁黑人女性的病例。建议在冯·希佩尔-林道病所见的肿瘤谱中考虑内淋巴囊乳头状腺癌。