Alzuhairy Sultan, Alkatan Hind M, Al-Rajhi Ali A
Ophthalmology Department, College of Medicine, Al-Qassim University, Riyadh, Saudi Arabia.
Department of Pathology and Laboratory Medicine, KKESH, Riyadh, Saudi Arabia.
Middle East Afr J Ophthalmol. 2015 Apr-Jun;22(2):179-85. doi: 10.4103/0974-9233.151975.
The aim was to determine the frequency and describe the main histopathologic features of corneal stromal dystrophy in Saudi Arabia.
A single-center, retrospective analysis of 193 corneal specimens diagnosed with stromal dystrophy. All samples were retrieved from the Histopathology Department at King Khaled Eye Specialist Hospital over a 10-year period (2002 to December 31, 2011). Cases of stromal dystrophy undergoing keratoplasty were included in the study. Routine histopathologic stains and specific stains were used to determine a diagnosis. The corresponding demographic data and basic clinical/surgical information were collected via chart review.
The study sample was comprised of 193 eyes. The final diagnoses were macular corneal dystrophy (MCD) in 180 (93.26%) eyes, granular corneal dystrophy (GCD) in 9 (4.66%) and lattice corneal dystrophy (LCD) in 4 (2.07%) eyes. The mean age at presentation was 27.03 years for MCD, 26.33 years for GCD and 53.75 years for LCD. The interval between diagnosis and surgical intervention was not statistically different between the macular and granular groups (P = 0.141). There was a positive family history for the MCD (37.22%) and GCD (44.44%) groups. All eyes underwent penetrating keratoplasty (PKP) except 10 MCD cases that underwent lamellar keratoplasty. Diffuse stromal deposits were present in 87.2% of MCD corneas and 66.67% of GCD corneas. Seventeen eyes with MCD were misdiagnosed as GCD. None of the LCD cases were clinically identified since all of these cases were diagnosed as corneal scarring. In eyes with MCD that underwent PKP, there was diffuse stromal involvement (in 87.22% eyes) and changes in Descemet's membrane (in 53.5% eyes).
This pathological study suggested that MCD was the most common corneal stromal dystrophy that required keratoplasty in Saudi Arabia. Patient with MCD and GCD presented at a significantly younger age than LCD. The clinical diagnosis of MCD is not achieved in all cases likely due to a more severe phenotype in the Saudi population or the presence of corneal scarring that is associated with previous trachoma, which obscures the classical appearance of LCD. We believe that PKP is first-line surgical treatment, especially for MCD because it involves all corneal layers. However, deep stromal involvement and changes in Descemet's membrane in MCD should be considered when selecting the surgical procedure.
旨在确定沙特阿拉伯角膜基质营养不良的发病率,并描述其主要组织病理学特征。
对193例诊断为基质营养不良的角膜标本进行单中心回顾性分析。所有样本均取自哈立德国王眼科专科医院病理科,时间跨度为10年(2002年至2011年12月31日)。研究纳入接受角膜移植术的基质营养不良病例。采用常规组织病理学染色和特殊染色进行诊断。通过查阅病历收集相应的人口统计学数据和基本临床/手术信息。
研究样本包括193只眼。最终诊断为斑点状角膜营养不良(MCD)180只眼(93.26%),颗粒状角膜营养不良(GCD)9只眼(4.66%),格子状角膜营养不良(LCD)4只眼(2.07%)。MCD患者就诊时的平均年龄为27.03岁,GCD为26.33岁,LCD为53.75岁。斑点状和颗粒状组在诊断与手术干预之间的间隔无统计学差异(P = 0.141)。MCD组(37.22%)和GCD组(44.44%)有家族史阳性。除10例MCD患者行板层角膜移植术外,所有患者均接受了穿透性角膜移植术(PKP)。87.2%的MCD角膜和66.67%的GCD角膜存在弥漫性基质沉积物。17只MCD眼被误诊为GCD。由于所有LCD病例均被诊断为角膜瘢痕,因此临床上未识别出LCD病例。接受PKP的MCD眼中,存在弥漫性基质受累(87.22%的眼)和后弹力层改变(53.5%的眼)。
这项病理学研究表明,MCD是沙特阿拉伯最常见的需要角膜移植的角膜基质营养不良。MCD和GCD患者的发病年龄明显低于LCD患者。并非所有MCD病例都能实现临床诊断,这可能是由于沙特人群中该疾病的表型更为严重,或者存在与既往沙眼相关的角膜瘢痕,从而掩盖了LCD的典型表现。我们认为PKP是一线手术治疗方法,尤其是对于MCD,因为它涉及角膜的所有层面。然而,在选择手术方式时,应考虑MCD中深层基质受累和后弹力层改变的情况。