Raafat F, Smith K, Halloran E A, Lacy D
Department of Pathology, Birmingham Children's Hospital, UK.
Pediatr Pathol. 1991 May-Jun;11(3):413-20. doi: 10.3109/15513819109064777.
Until 17 years ago the diagnosis of the cerebrohepatorenal Zellweger syndrome (ZS) rested largely on clinical grounds confirmed by pathologic findings at autopsy. The observation that peroxisomes are not detectable morphologically or histochemically in liver or kidney of patients with this syndrome gave histopathologists the opportunity to make the diagnosis of this complex syndrome at biopsy. Catalase reaction of the peroxisomes can be used as a rapid and accurate method to differentiate between ZS and other clinical conditions in which the peroxisomes are present in normal or reduced number. We describe two patients in whom the diagnosis of ZS was made by the absence of histochemical staining for catalase in a liver biopsy. The findings were subsequently confirmed using standard biochemical tests.
直到17年前,脑肝肾齐-韦二氏综合征(ZS)的诊断很大程度上基于临床依据,并通过尸检的病理结果得以证实。观察发现,该综合征患者的肝脏或肾脏中,过氧化物酶体在形态学或组织化学上均无法检测到,这使组织病理学家有机会在活检时对这种复杂综合征做出诊断。过氧化物酶体的过氧化氢酶反应可作为一种快速准确的方法,用于区分ZS与其他过氧化物酶体数量正常或减少的临床病症。我们描述了两名患者,他们通过肝活检中过氧化氢酶组织化学染色缺失而被诊断为ZS。随后通过标准生化检测证实了这些发现。