Kozłowski T, Cybulska M, Błaszczyk B, Krajewska M, Jeśman C
Nicolaus Copernicus University, Faculty of Biology and Environment Protection, Department of Anthropology, Lwowska 1, 87-100 Toruń, Poland.
Medical University of Łódź, Faculty of Military Medicine with the Division of Physiotherapy, History of Sciences and Military Medicine Department, Łódź, Poland.
Homo. 2014 Oct;65(5):400-22. doi: 10.1016/j.jchb.2014.08.001. Epub 2014 Aug 19.
of morphological and tomographic (CT) studies of the skull that was found in the crypt of the Silesian Piasts in the St. Jadwiga church in Brzeg (Silesia, Poland) are presented and discussed here. The established date of burial of probably a 20-30 years old male was 16th-17th century. The analyzed skull showed premature obliteration of the major skull sutures. It resulted in the braincase deformation, similar to the forms found in oxycephaly and microcephaly. Tomographic analysis revealed gross pathology. Signs of increased intracranial pressure, basilar invagination and hypoplasia of the occipital bone were observed. Those results suggested the occurrence of the very rare Arnold-Chiari syndrome. Lesions found in the sella turcica indicated the development of pituitary macroadenoma, which resulted in the occurrence of discreet features of acromegaly in the facial bones. The studied skull was characterized by a significantly smaller size of the neurocranium (horizontal circumference 471 mm, cranial capacity ∼ 1080 ml) and strongly expressed brachycephaly (cranial index=86.3), while its height remained within the range for non-deformed skulls. A narrow face, high eye-sockets and prognathism were also observed. Signs of alveolar process hypertrophy with rotation and displacement of the teeth were noted. The skull showed significant morphological differences compared to both normal and other pathological skulls such as those with pituitary gigantism, scaphocephaly and microcephaly.
本文展示并讨论了在波兰布热格(西里西亚)圣雅德维加教堂西里西亚皮亚斯特家族墓穴中发现的头骨的形态学和断层扫描(CT)研究结果。据推测,该男性死者年龄在20至30岁之间,下葬时间为16至17世纪。经分析,该头骨主要颅骨缝过早闭合,导致颅腔变形,类似于尖头畸形和小头畸形的形态。断层扫描分析显示存在严重病变,观察到颅内压升高、基底凹陷和枕骨发育不全的迹象。这些结果提示可能发生了极为罕见的阿诺德 - 奇亚里综合征。蝶鞍区发现的病变表明垂体大腺瘤的发展,这导致面部骨骼出现肢端肥大症的细微特征。所研究的头骨特点是脑颅尺寸明显较小(水平周长471毫米,颅容量约1080毫升),短头畸形明显(颅指数 = 86.3),而其高度仍在未变形头骨的范围内。还观察到面部狭窄、眼眶高和凸颌。注意到牙槽突肥大伴有牙齿旋转和移位的迹象。与正常头骨以及其他病理性头骨(如垂体巨人症、舟状头畸形和小头畸形的头骨)相比,该头骨显示出明显的形态差异。