Adenomyomas of the Gallbladder: An Analysis of Frequency, Clinicopathologic Associations, and Relationship to Carcinoma of a Malformative Lesion.

IF 3.7 3区 医学 Q2 MEDICAL LABORATORY TECHNOLOGY
Nevra Dursun, Bahar Memis, Burcin Pehlivanoglu, Orhun Cig Taskin, Oguzhan Okcu, Gizem Akkas, Pelin Bagci, Serdar Balci, Burcu Saka, Juan Carlos Araya, Enrique Bellolio, Juan Carlos Roa, Kee-Taek Jang, Hector Losada, Shishir K Maithel, Juan Sarmiento, Michelle D Reid, Jin-Young Jang, Jeanette D Cheng, Olca Basturk, Jill Koshiol, N Volkan Adsay
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引用次数: 0

Abstract

Context.—: The nature and associations of gallbladder (GB) "adenomyoma" (AM) remain controversial. Some studies have attributed up to 26% of GB carcinoma to AMs.

Objective.—: To examine the true frequency, clinicopathologic characteristics, and neoplastic changes in GB AM.

Design.—: Cholecystectomy cohorts analyzed were 1953 consecutive cases, prospectively with specific attention to AM; 2347 consecutive archival cases; 203 totally embedded GBs; 207 GBs with carcinoma; and archival search of institutions for all cases diagnosed as AM.

Results.—: Frequency of AM was 9.3% (19 of 203) in totally submitted cases but 3.3% (77 of 2347) in routinely sampled archival tissue. A total of 283 AMs were identified, with a female to male ratio = 1.9 (177:94) and mean size = 1.3 cm (range, 0.3-5.9). Most (96%, 203 of 210) were fundic, with formed nodular trabeculated submucosal thickening, and were difficult to appreciate from the mucosal surface. Four of 257 were multifocal (1.6%), and 3 of 257 (1.2%) were extensive ("adenomyomatosis"). Dilated glands (up to 14 mm), often radially converging to a point in the mucosa, were typical. Muscle was often minimal, confined to the upper segment. Nine of 225 (4%) revealed features of a duplication. No specific associations with inflammation, cholesterolosis, intestinal metaplasia, or thickening of the uninvolved GB wall were identified. Neoplastic change arising in AM was seen in 9.9% (28 of 283). Sixteen of 283 (5.6%) had mural intracholecystic neoplasm; 7 of 283 (2.5%) had flat-type high-grade dysplasia/carcinoma in situ. Thirteen of 283 cases had both AM and invasive carcinoma (4.6%), but in only 5 of 283 (1.8%), carcinoma arose from AM (invasion was confined to AM, and dysplasia was predominantly in AM).

Conclusions.—: AMs have all the features of a malformative developmental lesion, and may not show a significant muscle component (ie, the name "adeno-myoma" is partly a misnomer). While most are innocuous, some pathologies may arise in AMs, including intracholecystic neoplasms, flat-type high-grade dysplasia or carcinoma in situ, and invasive carcinoma (1.8%, 5 of 283). It is recommended that gross examination of GBs include serial slicing of the fundus for AM detection and total submission if one is found.

胆囊腺肌瘤:胆囊腺肌瘤:发病率、临床病理关联以及与畸形病变癌的关系分析。
背景胆囊(GB)"腺肌瘤"(AM)的性质和关联仍存在争议。一些研究将高达 26% 的胆囊癌归因于 AM:研究胆囊腺肌瘤的真实发生率、临床病理特征和肿瘤性变化:分析的胆囊切除术队列包括 1953 例连续病例,前瞻性地特别关注 AM;2347 例连续档案病例;203 例完全嵌顿的 GB;207 例发生癌变的 GB;以及对所有诊断为 AM 的病例进行机构档案检索:结果:在全部送检病例中,AM的发生率为9.3%(203例中的19例),而在常规取样的档案组织中,AM的发生率为3.3%(2347例中的77例)。共鉴定出 283 个 AM,雌雄比例为 1.9(177:94),平均大小为 1.3 厘米(范围为 0.3-5.9)。大多数(96%,210 个中的 203 个)为胃底型,粘膜下增厚形成结节状小梁,从粘膜表面很难观察到。257 例中有 4 例(1.6%)是多灶性的,257 例中有 3 例(1.2%)是广泛性的("腺肌瘤病")。腺体扩张(最多 14 毫米)是典型症状,通常呈放射状汇聚到粘膜的某一点。肌肉通常很少,仅限于上段。225 例中有 9 例(4%)显示有重复特征。未发现与炎症、胆固醇沉积、肠化生或未受累的胃壁增厚有特殊关联。9.9%的病例(283 例中的 28 例)发生了 AM 肿瘤。283例中有16例(5.6%)为壁内胆囊肿瘤;283例中有7例(2.5%)为扁平型高级别发育不良/原位癌。283例中有13例(4.6%)同时患有AM和浸润癌,但283例中只有5例(1.8%)的癌细胞来自AM(浸润局限于AM,发育不良主要发生在AM):AM具有畸形发育病变的所有特征,但可能没有明显的肌肉成分(即 "腺肌瘤 "这一名称在一定程度上是一种误称)。虽然大多数腺肌瘤是无害的,但也可能出现一些病变,包括囊内肿瘤、扁平型高级别发育不良或原位癌以及浸润性癌(1.8%,283 例中有 5 例)。建议在对 GB 进行大体检查时,对眼底进行连续切片,以检测 AM,如果发现 AM,则将其全部送检。
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来源期刊
CiteScore
9.20
自引率
2.20%
发文量
369
审稿时长
3-8 weeks
期刊介绍: Welcome to the website of the Archives of Pathology & Laboratory Medicine (APLM). This monthly, peer-reviewed journal of the College of American Pathologists offers global reach and highest measured readership among pathology journals. Published since 1926, ARCHIVES was voted in 2009 the only pathology journal among the top 100 most influential journals of the past 100 years by the BioMedical and Life Sciences Division of the Special Libraries Association. Online access to the full-text and PDF files of APLM articles is free.
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