Ferrara B E, Hazell S, Parker T H, Rutland E D
South Med J. 1985 May;78(5):528-32. doi: 10.1097/00007611-198505000-00007.
Although parathyroid cyst has been infrequently reported until the past decade, its presumed rarity is attributed to nonrecognition. First reported in 1905, only 58 cases of parathyroid cyst had been documented in the world literature by 1967. Since then, however, substantial literature about this entity has been accumulating. The three cases we are reporting bring the cumulative total to 149. All three have been examined histologically and treated by aspiration or surgical excision. There is confusion clinically with thyroid cysts, and assay of fluid aspirate for parathormone and thyroxine may not accurately distinguish the origin of the cyst. Tissue diagnosis is confirmatory. Parathyroid cysts may be developmental, arising from vestigial remnants of the third and fourth branchial clefts; or coalescence of microcysts with associated hypersecretion may enlarge into macrocysts; or an adenoma may degenerate into a pseudocyst. Hyperparathyroidism, if present, is associated with only the last two.
尽管直到过去十年甲状旁腺囊肿才鲜有报道,但推测其罕见是由于未被识别。1905年首次报道,到1967年世界文献中仅记载了58例甲状旁腺囊肿。然而,从那时起,关于这个实体的大量文献不断积累。我们报告的这三例使累积总数达到149例。所有三例均进行了组织学检查,并通过抽吸或手术切除进行了治疗。临床上与甲状腺囊肿存在混淆,对抽吸液进行甲状旁腺素和甲状腺素检测可能无法准确区分囊肿的来源。组织诊断具有确诊性。甲状旁腺囊肿可能是发育性的,起源于第三和第四鳃裂的残留遗迹;或者微囊肿合并伴有分泌过多可能扩大形成大囊肿;或者腺瘤可能退化为假性囊肿。如果存在甲状旁腺功能亢进,仅与后两种情况相关。