Peculiar inflammatory cutaneous metastasis from stomach adenocarcinoma
Peculiar inflammatory cutaneous metastasis from stomach adenocarcinoma
复制标题
胃腺癌的特殊炎症性皮肤转移
DOI:
10.1111/j.1365-2133.1997.tb02179.x
复制
发表时间:
1997
影响因子:
10.3
通讯作者:
A. Sungur
中科院分区:
文献类型:
--
作者:
S. Şahin;U. Hindioḡlu;M. Benekli;B. Sivri;C. Sökmensüer;A. Sungur
Aortic coarctation and supraumbilical raphe are other mallbrmations more frequently observed in patients with GFH than in normal children.'"'* Overlapping of all these anomalies has been reported in some instances, and ail may present in the same child. In this context, a new 3C syndrome was defined by Goh and Lo.' as the concurrence of cerebellar hypoplasia. cavernous haemangioma. and aortic coarctation in the same patient. Another term was proposed by Frieden et fl/.r on observing that a more complex range of abnormalities may also occur. They proposed the acronym PHACE syndrome, to denote the major features of this neurocutaneous syndrome: P. posterior fossa malformations: H. haemangiomas; A. arterial abnormalities; C. coarctation of the aorta and cardiac defects; and E. eye abnormalities. These authors arrived at this acronym after describing two cases and reviewing the literature. GFH was present in all patients with this syndrome: SS% of them were females, as in our case."'"' 74% had a brain malformation of the posterior fossa. 41% presented arterial anomalies. 2b% had cardiac or aortic malformations and 26% presented unusual eye abnormalities."