罗马帝国时代的骨畸形和骨骼畸形。

Medicina nei secoli Pub Date : 2014-01-01
Simona Minozzi, Paola Catalano, Walter Pantano, Carla Caldarini, Gino Fornaciari
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引用次数: 0

摘要

本文描述了一些受骨骼畸形影响的个体,导致“怪异”的外观。这些遗骸是在罗马领土的大型考古发掘中发现的,由罗马考古遗产特别监督局在过去几年中进行,可以追溯到帝国时代。第一例报告的病例涉及两种相反影响的生长障碍:一例为侏儒症,另一例为巨人症。前者涉及一名来自Collatina墓地的年轻人,他的四肢非常短且畸形,这使得他被诊断为发育不良侏儒症,这是一种罕见的先天性疾病,将身高限制在130厘米以下。后一个病例来自菲德纳的Torre Serpentana墓地,而是指一个身高非常高的年轻人,大约204厘米,患有巨人症,这种罕见的情况似乎与垂体腺瘤引起的激素功能障碍有关。第三例涉及影响脊柱并导致严重畸形的关节疾病。这具骨骼是在Collatina墓地发现的,属于一位患有强直性脊柱炎的老妇人。最后,最后一个非常特殊的案例与在马尔诺姆城堡墓地发现的一个人有关。这具骨骼残骸属于一名成年男子,其颞下颌关节完全融合,这损害了咀嚼功能,并导致颌面复合体严重变形。详细描述了这些病例以及这些畸形在社会背景下可能产生的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Bone deformities and skeletal malformations in the Roman Imperial Age.

This paper describes some cases of individuals affected by skeletal deformities resulting in "freak" appearance. The skeletal remains were found during large archaeological excavations in the Roman territory, carried out by the Special Superintendence to the Archeological Heritage of Rome in the last years, dated back to the Imperial Age. The first cases reported are referred to two growth disorders with opposite effects: a case of dwarfism and another of gigantism. The former concerns a young man from the Collatina necropolis with very short and malformed limbs, which allowed a diagnosis of acondroplasic dwarfism, a rare congenital disorder that limits height below 130 cm. The latter case comes from the necropolis of Torre Serpentana in Fidenae, and is instead referred to a young person of very high stature, about 204 cm, suffering from Gigantism, a rare condition which in this case seems to have been linked to a hormonal dysfunction due to a pituitary adenoma. A third case regards a joint disease affecting the vertebral column and causing severe deformities. The skeleton was found in the Collatina necropolis and belongs to an old woman, suffering from ankylosing spondylitis. Finally, the last and very peculiar case is related to an individual recovered in the necropolis of Castel Malnome. The skeletal remains belong to an adult man with a complete fusion of the temporo-mandibular joint, which compromised mastication and caused severe deformation of the maxillofacial complex. These cases are described in detail together with the possible implications that these deformities could have on in the social context.

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