Morad N A, al-Malki T, e-Tahir M
Department of Pathology, College of Medicine, King Saud University, Abha, Saudi Arabia.
Pathology. 1997 May;29(2):218-20. doi: 10.1080/00313029700169904.
This case report describes the unusual occurrence of congenital cystic adenomatoid malformation (CCAM) type 2 in an intra-abdominal pulmonary sequestration as a cause of diagnostic difficulties. The mass was discovered incidentally during a routine prenatal ultrasound in an infant with no other congenital malformation. Extralobar pulmonary sequestrations (EPS) located in the abdomen are rarely diagnosed prior to excision. The presence of CCAM type 2 in this situation might impose difficulties in histologic diagnosis of EPS, especially at the time of frozen section as happened in this case. To our knowledge this case is the sixth reported case of intra-abdominal EPS and the sixteenth case of EPS histologically displaying the feature of CCAM type 2. Pathologists should be aware that EPS in any location might display histologic features of CCAM type 2 even if the EPS is intra-abdominal.
本病例报告描述了先天性囊性腺瘤样畸形(CCAM)2型罕见地发生于腹腔内肺隔离症中,导致诊断困难。该肿块是在一名无其他先天性畸形的婴儿进行常规产前超声检查时偶然发现的。位于腹部的肺叶外型肺隔离症(EPS)在切除前很少被诊断出来。在这种情况下CCAM 2型的存在可能会给EPS的组织学诊断带来困难,尤其是在本例中进行冰冻切片检查时。据我们所知,本病例是第六例报道的腹腔内EPS病例,也是第十六例组织学显示CCAM 2型特征的EPS病例。病理学家应意识到,任何部位的EPS即使位于腹腔内,也可能表现出CCAM 2型的组织学特征。