Meena Manju, Martin Peter A, Abouseif Claire, Bullpitt Peter
Oculoplastic Unit, Department of Ophthalmology, Sydney Hospital and Sydney Eye Hospital , Macquarie Street, Sydney, NSW , Australia and.
Orbit. 2014 Oct;33(5):395-8. doi: 10.3109/01676830.2014.907813. Epub 2014 Jun 9.
To report an unusual presentation of a case of Lymphomatoid papulosis(LyP) in a young girl.
A 14-year-old female presented with a history of swelling of the left upper eyelid of two weeks duration. There was a history of trivial trauma prior to the swelling. The patient was diagnosed as having pre-septal cellulitis elsewhere and was put on oral antibiotics. The lesion was non-responsive to oral antibiotics. The patient was then referred to our hospital. Ocular examination revealed an elevated lesion measuring 15 mm × 10 mm on the left upper eyelid, associated with pre-septal swelling and induration. Ocular movements were normal. The anterior and posterior segment examination was normal. Incision biopsy was done from the eyelid lesion. Multiple cutaneous lesions were also biopsied.
The histopathology examination confirmed the diagnosis of lymphomatoid papulosis type C. Dermatological and systemic evaluation ruled out the other aggressive forms of CD30(+) lymphoid proliferation.
We report an unusual presentation of lymphomatoid papulosis(LyP) type C in a young girl. Complete systemic work up and histopathological evaluation is mandatory in cases of suspicious lesions, not responding to conservative treatment.
报告一名年轻女孩淋巴瘤样丘疹病(LyP)的不寻常表现。
一名14岁女性,有左上眼睑肿胀两周的病史。肿胀前有轻微外伤史。该患者在其他地方被诊断为眶隔前蜂窝织炎,并接受口服抗生素治疗。病变对口服抗生素无反应。随后患者被转诊至我院。眼部检查发现左上眼睑有一个15毫米×10毫米的隆起病变,伴有眶隔前肿胀和硬结。眼球运动正常。眼前段和后段检查均正常。对眼睑病变进行了切开活检。还对多个皮肤病变进行了活检。
组织病理学检查确诊为C型淋巴瘤样丘疹病。皮肤科和全身评估排除了其他侵袭性形式的CD30(+)淋巴增殖性疾病。
我们报告了一名年轻女孩C型淋巴瘤样丘疹病(LyP)的不寻常表现。对于可疑病变且对保守治疗无反应的病例,必须进行全面的全身检查和组织病理学评估。