Assmann A, Mandt N, Geilen C C, Blume-Peytavi U
Department of Dermatology, University Medical Center Charité, Medical Faculty of the Humboldt University, Schumannstr. 20-21, 10117 Berlin, Germany.
Eur J Dermatol. 2001 Nov-Dec;11(6):576-9.
We report a 5-year-old boy presenting with multiple elastic type nevi and osteopoikilosis who was diagnosed as having Buschke-Ollendorff syndrome at an early age. Connective tissue lesions may present as the main symptom of varying clinical entities with different outcomes. Differential diagnosis includes papular elastorrhexis, fibroelastolytic papules of the neck, papular acne scars, and late onset focal dermal elastosis. Rare genodermatoses, i.e. Buschke-Ollendorff syndrome, pseudoxanthoma elasticum, juvenile hyaline fibromatosis and familiar cutaneous collagenoma should be carefully evaluated to provide appropriate genetic counseling and to avoid unnecessary treatment procedures.
我们报告了一名5岁男孩,他患有多发性弹性型痣和骨斑点症,早年被诊断为布希克-奥伦多夫综合征。结缔组织病变可能是不同临床实体的主要症状,预后各异。鉴别诊断包括丘疹性弹性组织离解、颈部纤维弹性组织溶解性丘疹、丘疹性痤疮瘢痕和迟发性局限性皮肤弹性组织变性。对于罕见的遗传性皮肤病,即布希克-奥伦多夫综合征、弹性假黄瘤、青少年透明纤维瘤病和家族性皮肤胶原瘤,应仔细评估,以提供适当的遗传咨询并避免不必要的治疗程序。