Ekblom Anna Gerber, Laurell Tobias, Arner Marianne
Department of Clinical Science and Education, Södersjukhuset, Section of Hand Surgery, Stockholm, Sweden.
J Hand Surg Am. 2010 Nov;35(11):1742-54. doi: 10.1016/j.jhsa.2010.07.007. Epub 2010 Oct 20.
There are few true epidemiological studies of congenital anomalies of the upper limb (CULA) on total populations in the literature, and most incidence studies are hospital based. The purposes of this study were to describe the epidemiology and classify all CULA in a region of Sweden during an 11-year period.
Between 1997 and 2007, there were 261,914 live births in the Stockholm region. A total of 562 children born during this period were found to have CULA. From medical records and available radiographs, all cases were analyzed regarding the type of congenital anomaly, gender, laterality, occurrence among relatives, associated non-hand anomalies, and syndromes. All 585 main anomalies were classified according to the International Federation of Societies for Surgery of the Hand classification. Individuals with right- and left-side main anomalies belonging to different categories were counted as having 2 anomalies.
The recorded incidence of CULA was 21.5 per 10,000 live births. Of the 562 children, 304 were boys. The anomalies affected the right side only in 169 children, the left side only in 186, and both sides in 207. Non-hand anomalies were recorded in 129 children, most commonly in the lower limbs. In 99 children, there was a known occurrence among relatives. Failure of differentiation was the most common category (276 of 585) followed by duplication (155 of 585), failure of formation (103 of 585), undergrowth (18 of 585), generalized abnormalities and syndromes (14 of 585), overgrowth (10 of 585), and constriction ring syndrome (9 of 585).
The incidence of CULA in our region was similar to the only previously comparable total population study from Western Australia. The minor differences in incidences between the categories according to the International Federation of Surgical Societies of the Hand may be due to variations in classification strategy. The results of the present study can be used as a reference of CULA in a total population.
文献中针对全人群上肢先天性畸形(CULA)的真正流行病学研究较少,大多数发病率研究是以医院为基础的。本研究的目的是描述瑞典某地区11年间CULA的流行病学情况并对所有CULA进行分类。
1997年至2007年期间,斯德哥尔摩地区共有261,914例活产儿。在此期间出生的562名儿童被发现患有CULA。根据病历和现有的X光片,对所有病例的先天性畸形类型、性别、侧别、亲属中的发病情况、相关的非手部畸形以及综合征进行了分析。所有585例主要畸形均按照国际手外科学会联合会的分类进行分类。右侧和左侧主要畸形属于不同类别的个体被计为患有2种畸形。
记录的CULA发病率为每10,000例活产儿中有21.5例。在这562名儿童中,304名是男孩。这些畸形仅影响右侧的有169名儿童,仅影响左侧的有186名,双侧都受影响的有207名。129名儿童记录有非手部畸形,最常见于下肢。99名儿童的亲属中有已知发病情况。分化失败是最常见的类别(585例中的276例),其次是重复畸形(585例中的155例)、形成失败(585例中的103例)、发育不全(585例中的18例)、全身性异常和综合征(585例中的14例)、过度生长(585例中的10例)以及环状缩窄综合征(585例中的9例)。
我们地区CULA的发病率与之前西澳大利亚唯一一项可比的全人群研究相似。根据国际手外科学会联合会分类,各类别发病率的细微差异可能归因于分类策略的不同。本研究结果可作为全人群中CULA的参考。