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我院曾收治一例先天性耳廓重复畸形,现报道如下: 患儿女,1(8/12)岁,因颈部两侧对称性扁形肿物渐大一年零八个月。于1990年11月入院。患儿出生时即见颈两侧中上部各有一对称性的扁形肿物突起皮肤。大小如半个花生米大,柔软。扪及内有硬性物。无任何症状。肿物随年龄增长而向外呈扁形增大。母亲怀孕时无毒物接触史。入院查:发育正常,营养佳,两耳廓、耳道、听力均正常。颈两侧距下颌角后下约3cm处各有一个对称性的扁形肿物,约长2cm,宽1.2cm,厚0.2cm。皮肤柔软。扪及内有扁形软骨样组织,硬度如耳廊软骨,深部与胸锁乳突肌相连。其余
A congenital auricular repeat deformity was admitted in our hospital and is reported as follows: Children and children, 1 (8/12) years old, have symmetrical flat masses on both sides of the neck gradually enlarged for one year and eight months. In November 1990 admitted. Children born at that time to see both sides of the neck in the upper part of a symmetrical flat tumor protruding skin. If the size of a large peanut, soft. Palpable with hard objects. No symptoms. The tumor grows flat outward with age. The mother had no history of exposure to poison during pregnancy. Admission check: normal development, good nutrition, two ears, ear canal, hearing are normal. The neck on both sides of the mandibular angle after about 3cm at a symmetrical flat tumor, about 2cm long, 1.2cm wide and 0.2cm thick. Skin is soft A palpable flat cartilage-like tissue, such as the hardness of the ear corridor cartilage, deep sternocleidomastoid connected. the remaining