Department of Otolaryngology, New York University School of Medicine, New York, New York, USA.
Otol Neurotol. 2012 Sep;33(7):1201-6. doi: 10.1097/MAO.0b013e31825d97fa.
Jugular bulb abnormalities (JBA), such as jugular bulb diverticula (JBD) or large jugular bulbs, rarely present in the middle ear. We review a large series of temporal bone histopathologic specimens to determine their prevalence and present a series of cases of JB abnormalities involving the middle ear (JBME) that shed light on the probable mechanism for their development.
1,579 unique temporal bone specimens and individuals with radiographically-diagnosed JBME.
Histopathologic and clinical review of temporal bone specimens and patient presentations, radiographic findings, treatments and outcomes.
Shared characteristics of JBME.
There were 17 cases of JBME in 1,579 temporal bone (1.1%), of which, 15 involved the inferior mesotympanum below the level of the round window membrane (RWM), whereas 2 encroached upon the RWM or ossicles. In addition, 4 clinical cases of large JBME extending above RWM were encountered; these occurred in both sexes with ages spanning from young to old (7-66 yr). They presented with conductive hearing loss (n = 3), ear canal mass (n = 1), and intraoperative bleeding (n = 1). Radiologically, they had multiple diverticula of the JB on the side with JBME, with 1 patient demonstrating growth on serial imaging studies. All patients who underwent additional imaging had marked hypoplastic contralateral transverse sinus.
JBME abnormalities are rare, present across age groups, and may demonstrate serial growth over time. They are usually associated with multiple other diverticula within the same JB. Our clinical series suggests that JBME's development and uniquely aggressive behavior results from contralateral transverse sinus outflow obstruction.
颈静脉球异常(JBA),如颈静脉球憩室(JBD)或大颈静脉球,在中耳中很少见。我们回顾了大量颞骨组织病理学标本,以确定其患病率,并介绍了一系列涉及中耳的 JBA 异常(JBME)病例,这些病例阐明了其发展的可能机制。
1579 例独特的颞骨标本和影像学诊断为 JBME 的个体。
颞骨标本和患者表现、影像学发现、治疗和结果的组织病理学和临床回顾。
JBME 的共同特征。
在 1579 例颞骨中有 17 例 JBME,其中 15 例累及低于圆窗膜(RWM)水平的中下鼓室,而 2 例侵犯 RWM 或听小骨。此外,还遇到了 4 例大 JBME 延伸至 RWM 以上的临床病例;这些病例发生在性别和年龄跨度从年轻到老年(7-66 岁)的个体中。他们表现为传导性听力损失(n=3)、耳道肿块(n=1)和术中出血(n=1)。影像学上,他们在 JBME 侧有多个 JB 憩室,其中 1 例在连续影像学研究中显示生长。所有接受额外影像学检查的患者均有明显的对侧横窦发育不全。
JBME 异常罕见,见于各年龄段,且可能随时间推移呈进行性生长。它们通常与同一 JB 内的多个其他憩室相关。我们的临床系列表明,JBME 的发展和独特的侵袭性行为是由于对侧横窦流出受阻所致。