Trattner A, Metzker A
Pediatric Dermatology Unit, Children's Medical Center of Israel, Petah Tiqva.
J Am Acad Dermatol. 1993 Nov;29(5 Pt 1):693-5. doi: 10.1016/0190-9622(93)70232-i.
We review our experience with nine patients with partial unilateral lentiginosis (PUL), a rare pigmentary disorder.
Our purpose was to define the characteristics of PUL and to discuss the differential diagnosis.
The records of nine patients with PUL were reviewed. A literature review on diagnosis, association with other disorders, and differential diagnosis is presented.
PUL is a rare benign disorder that has no known inheritance pattern and has no commonly associated abnormalities.
Careful history and physical examination may enable the distinction between PUL, nevus spilus, and other more serious genetic disorders associated with lentiginosis.
我们回顾了9例部分性单侧雀斑样痣(PUL)患者的病例,这是一种罕见的色素沉着障碍。
我们的目的是明确PUL的特征并讨论鉴别诊断。
回顾了9例PUL患者的病历。并对诊断、与其他疾病的关联以及鉴别诊断进行了文献综述。
PUL是一种罕见的良性疾病,尚无已知的遗传模式,也无常见的相关异常。
详细的病史和体格检查可能有助于区分PUL、斑痣和其他与雀斑样痣相关的更严重的遗传性疾病。