黄甲综合征——合并黄甲及胸腔积液的原发性淋巴水肿,为临床所罕见。近遇1例,报告如下。患者毛××,男性,32岁,住院号276426。双下肢粗肿20余年,伴气急11个月,于1987年12月7日入院。出生后即四肢粗壮,呈藕节状;幼年时下肢皮肤反复红肿、发热和腹股沟淋巴结肿大,用青霉素后症状消退。10岁左右下肢及阴囊皮肤逐渐增厚, Yellow A syndrome - a combination of Huang and pleural effusion of primary lymphedema, rare in clinical practice. Nearly one case, the report is as follows. Patient hair × ×, male, 32 years old, hospital number 276426. Lower extremity swelling more than 20 years, with acute gas 11 months, on December 7, 1987 admission. After birth, limbs stout, was lotus-like joints; juvenile lower limb skin repeatedly red and swollen, fever and inguinal lymph nodes, with penicillin symptoms subsided. 10-year-old lower extremity and scrotal skin gradually thickening,