School of Medicine, Loma Linda University, Loma Linda, CA, USA.
Division of Pediatric Surgery, Loma Linda University Children's Hospital, Loma Linda, CA, USA.
Am J Case Rep. 2023 Mar 24;24:e938248. doi: 10.12659/AJCR.938248.
BACKGROUND Lowe syndrome, also known as oculocerebrorenal syndrome, is a rare genetic condition caused by an X-linked mutation of the OCRL1 gene, with an estimated prevalence in the general population of approximately 1 in 500 000. It is a multisystem disorder most commonly affecting the eyes, central nervous system, and kidneys. These commonly manifest as congenital cataracts, intellectual disability, and proximal renal dysfunction (Fanconi-type). Epidermal lesions are an uncommon manifestation of this condition, and the association is not completely understood. CASE REPORT Here we present a case of a 9-year-old boy with Lowe syndrome who presented with multiple cystic masses found in the perianal region. An excision was then performed to remove the masses and found that the lesions were epidermal cysts, which are infrequently found in Lowe syndrome. After excision, the patient recovered uneventfully without complications. CONCLUSIONS While epidermal cysts are an uncommon manifestation that have been documented, our case remains unique given the location and associated symptoms of the lesions. At presentation, the constellation of pain and perianal masses was concerning for a malignant etiology. However, after diagnostic imaging was performed, these lesions were found to be epidermal cysts, an infrequent manifestation of Lowe syndrome. Few previous case reports described cystic lesions in association with Lowe syndrome, and none, to our knowledge, have described multiple symptomatic perianal lesions. This case is important to consider because epidermal cystic lesions can be found with this presentation and should be considered on differential diagnoses for dermatologic findings in Lowe syndrome patients.
Lowe 综合征,也称眼脑肾综合征,是一种罕见的遗传性疾病,由 OCRL1 基因突变引起,在普通人群中的患病率约为 1/500000。它是一种多系统疾病,最常影响眼睛、中枢神经系统和肾脏。这些疾病通常表现为先天性白内障、智力障碍和近端肾功能障碍(范可尼型)。皮肤病变是这种疾病的一种罕见表现,其关联尚未完全清楚。
在这里,我们报告了一例 9 岁 Lowe 综合征男孩,他出现了肛周区域的多个囊性肿块。随后进行了切除手术,发现病变为表皮囊肿,这种情况在 Lowe 综合征中并不常见。切除后,患者恢复顺利,无并发症。
虽然表皮囊肿是一种罕见的表现形式,但我们的病例由于病变的位置和相关症状仍然是独特的。在就诊时,疼痛和肛周肿块的组合令人担忧可能是恶性病因。然而,在进行了诊断性影像学检查后,这些病变被发现是表皮囊肿,这是 Lowe 综合征的一种不常见表现。以前很少有病例报告描述过与 Lowe 综合征相关的囊性病变,据我们所知,也没有描述过多个症状性肛周病变。这个病例很重要,因为在这种情况下可能会发现表皮囊性病变,在 Lowe 综合征患者的皮肤病学发现的鉴别诊断中应考虑到这些病变。