Department of Human Anatomy & Cell Biology, University of Liverpool, Liverpool, UK.
J Clin Pathol. 2010 Feb;63(2):186-8. doi: 10.1136/jcp.2009.071365.
Alkaptonuria (AKU) is a rare autosomal recessive condition caused by deficiency of the enzyme homogentisate 1,2 dioxygenase, resulting in widespread deposition of oxidised homogentisic acid (HGA) polymer, primarily in joint tissues but also in other connective tissues. Macroscopic pigmentation of connective tissues in AKU is well documented and is the end point of a process that is not understood. Deposition in less common regions may provide clues to the pigment formation process. This is the first report of detection of ochronotic pigment in acinar cells and lumina in the submandibular gland of a patient with AKU. Deposition was noted in the apical region of the cells. A lobar duct presented a large calculus with unusual deposits possibly associated with calcium salts. This report highlights the effect that local and intracellular factors may have on converting HGA into polymeric derivatives in the absence of an extracellular matrix.
尿黑酸尿症(AKU)是一种罕见的常染色体隐性遗传疾病,由 homogentisate 1,2 双加氧酶缺乏引起,导致广泛沉积氧化的 homogentisic 酸(HGA)聚合物,主要在关节组织中,但也在其他结缔组织中。AKU 中结缔组织的宏观色素沉着已有充分记录,这是一个尚未被理解的过程的终点。在不太常见的区域的沉积可能为色素形成过程提供线索。这是首例报道在 AKU 患者的颌下腺腺泡细胞和腔中检测到褐素的报告。沉积在细胞的顶区。一个小叶导管有一个大结石,有不寻常的沉积物,可能与钙盐有关。本报告强调了在没有细胞外基质的情况下,局部和细胞内因素可能对将 HGA 转化为聚合衍生物的影响。