Salivary gland aplasia with cleft lip and palate - A case report and review of the literature

被引：23
作者：
Matsuda, C [1 ]
Matsui, Y [1 ]
Ohno, K [1 ]
Michi, K [1 ]
机构：
[1] Showa Univ, Sch Dent, Dept Oral & Maxillofacial Surg 1, Ohta Ku, Tokyo 1458515, Japan
来源：
ORAL SURGERY ORAL MEDICINE ORAL PATHOLOGY ORAL RADIOLOGY AND ENDODONTICS | 1999年 / 87卷 / 05期
关键词：
D O I：
10.1016/S1079-2104(99)70140-X
中图分类号：
R78 [口腔科学];
学科分类号：
1003 ;
摘要：
We report the case of a patient with lifelong symptoms of xerostomia and a repaired bilateral cleft lip and palate. The clinical evaluation demonstrated aplasia of the major salivary glands. A review of the literature pertaining to salivary gland aplasia is presented, along with a summary of the data regarding patient gender, defect sites, hereditary background, and combined manifestations. The diagnostic methods, possible pathogenesis, and management are also discussed.
引用
收藏
页码：594 / 599
页数：6
相关论文
共 43 条
[1]   CONGENITAL ABSENCE OF SUB-MAXILLARY GLAND DETECTED ON TC-99M-PERTECHNETATE THYROID IMAGING [J].
ABDELDAYEM, HM .
CLINICAL NUCLEAR MEDICINE, 1978, 3 (11) :442-442
[2]  
ASHIKAGAYA M, 1991, DENT RADIOLOGY, V31, P143
[3]   Multiple congenital anomalies in a stillborn infant [J].
Ashley, LM ;
Richardson, GE .
ANATOMICAL RECORD, 1943, 86 (04) :457-471
[4]  
AUSTIN T, 1936, ILLINOIS MED J, V69, P124
[5]  
BECKER W, 1960, FORTSCHR KIEFER GESI, V6, P198
[6]  
BLACKMAR FB, 1925, AM J OPHTHALMOL, V8, P139
[7]  
Bruno P, 1894, ATT 11 C MED, V2, P62
[8]  
DEMORAESGREY J, 1937, ANN ANAT PATHOL, V14, P871
[9]  
ENTIN M A, 1958, Plast Reconstr Surg Transplant Bull, V21, P461, DOI 10.1097/00006534-195806000-00006
[10]  
FABER M, 1942, ACTA PAEDIATR, V30, P148
12345