Mucocele-like lesion

  • 文章类型: Case Reports
    在临床上,口腔淋巴瘤非常罕见,并且经常难以识别。粘膜相关淋巴组织(MALT)淋巴瘤是一类多样化的淋巴瘤,以前被认为是由位于边缘区的B细胞形成的。围绕着B细胞滤泡和周围的淋巴上皮。像胃这样的结外器官,甲状腺,大唾液腺是它们最常出现的地方。因此,它们被准确鉴定为结外边缘区B细胞淋巴瘤(ENMZL)。本报告介绍一例53岁女性下唇肿胀,经临床诊断为边缘低度B细胞非霍奇金淋巴瘤,组织病理学,和免疫检查。非霍奇金淋巴瘤的诊断可以通过病变发展早期的病理检查和活检来辅助。牙医在早期诊断过程中起着关键作用。
    In a clinical context, oral lymphomas are very uncommon and frequently challenging to identify. Mucosa-associated lymphoid tissue (MALT) lymphomas are a diverse category of lymphomas that were formerly believed to be formed from B-cells located in the marginal zone, which surrounds B-cell follicles and the surrounding lymphoepithelium. Extranodal organs like the stomach, thyroid, and large salivary glands are where they most frequently appear. As a result, they are accurately identified as extranodal marginal zone B-cell lymphomas (ENMZL). This report presents a case of a 53-year-old female with lower lip swelling, which was diagnosed as a case of marginal low-grade B-cell non-Hodgkin\'s lymphoma after clinical, histopathological, and immunological examinations. Non-Hodgkin\'s lymphoma diagnosis can be aided by pathological examination and biopsy performed early in the lesion\'s development. The dentist has a key role to play in the early diagnosis process.
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  • 文章类型: Review
    乳腺粘液囊肿样病变(MLLs)是罕见的病变,描述为扩张,与周围基质中的破裂和细胞外粘蛋白相关的粘蛋白填充的囊肿。这些病变是临床关注的,因为它们可以与一系列非典型和恶性发现共存,包括不典型的导管增生,导管原位癌,和浸润性癌,包括粘液性癌。MLLs的影像学表现是非特异性和多样性的,尽管最常见的初始发现是乳房X线照相术上偶然发现的粗糙异质钙化。偶尔,可以发现有或没有钙化的不对称性或肿块,并且此类MLLs在切除时具有较高的恶性升级率。病理结果通常是描述性的,因为从经皮活检获得的小样本,首要考虑是报告任何相关的非典型性,包括不典型的导管增生。文献中一致认为,活检中具有异型性的MLLs应进行切除,因为平均报告17.5%(20/114)的恶性率上升。无异型MLL的升级率平均为4.1%(14/341)。因此,影像学监测可能是对无异型MLLs逐例切除的合理选择.我们回顾MLL成像发现,病理结果,和临床治疗,并提出了我们机构的3例病例,以增加有关这些罕见病变的文献。
    Mucocele-like lesions (MLLs) of the breast are rare lesions described as dilated, mucin-filled cysts associated with rupture and extracellular mucin in the surrounding stroma. These lesions are of clinical concern because they can coexist with a spectrum of atypical and malignant findings, including atypical ductal hyperplasia, ductal carcinoma in situ, and invasive carcinoma including mucinous carcinoma. Imaging findings of MLLs are nonspecific and varied, although the most common initial finding is that of incidental coarse heterogeneous calcifications on mammography. Occasionally, an asymmetry or mass may be found with or without calcifications, and such MLLs have a higher rate of upgrade to malignancy at excision. Pathology findings are often descriptive given the small sample received from percutaneous biopsy, and the primary consideration is to report any associated atypia, including atypical ductal hyperplasia. There is consensus in the literature that MLLs with atypia on biopsy should undergo excision because of the average reported 17.5% (20/114) upgrade rate to malignancy. The upgrade rate for MLLs without atypia averages 4.1% (14/341). Therefore, imaging surveillance may be a reasonable alternative to excision for MLLs with no atypia on a case-by-case basis. We review MLL imaging findings, pathology findings, and clinical management and present 3 cases from our institution to add to the literature on these rare lesions.
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  • 文章类型: Case Reports
    乳腺粘液囊肿样病变(MLLs)是罕见的肿瘤,以扩张为特征,粘蛋白填充的上皮导管或囊肿,可以破裂并将其内容物排出到周围的基质中。它们经常与非典型性有关,发育不良的变化,and,最近,癌前和恶性状况,如非典型导管增生,导管癌,浸润性癌,或者黏液性癌.由于大量的粘蛋白和低细胞性,MLLs的恶性潜力通常很难从芯针活检的初始组织学评估中确定。因此,在最初的介绍中,MLLs应手术切除并彻底评估恶性肿瘤。在本文中,我们提出了一个罕见的MLL病例,并探讨了放射学,组织学,致癌潜力,诊断评估,并建议对病情进行管理。
    Mucocele-like lesions (MLLs) of the breast are rare neoplasms characterized by dilated, mucin-filled epithelial ducts or cysts that can rupture and expel their contents into the surrounding stroma. They are frequently associated with atypia, dysplastic change, and, more recently, pre-malignant and malignant conditions like atypical ductal hyperplasia, ductal carcinoma, invasive carcinoma, or mucinous carcinoma. The malignant potential of MLLs is often challenging to determine from the initial histologic evaluation of a core-needle biopsy due to copious mucin and low cellularity. Therefore, at initial presentation, MLLs should be surgically excised and thoroughly evaluated for malignancy. In this paper, we present a rare case of an MLL and explore the radiology, histology, carcinogenic potential, diagnostic evaluation, and suggested management of the condition.
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  • 文章类型: Journal Article
    背景:影像引导核心活检诊断的高危乳腺病变的处理仍存在争议。我们实施了一个由乳腺病理学家参加的高风险乳腺会议,成像仪,和外科医生前瞻性地审查所有当代病例,以便为手术切除或每隔6个月随访至少2年的影像学提供共识建议。
    方法:5月之间,2015年6月,2019年,讨论了127个高危病变。在这127个案例中,116具有一致的放射学-病理学(rad-path)发现。其余11例患者的rad-path结果不一致。在116个和谐案例中,由于在分析之前缺乏第一次成像随访,6例被排除。在剩下的110名患者中,43例导管不典型增生(ADH),12例小叶原位癌(LCIS),19例不典型小叶增生(ALH),33有放射状疤痕(RS),2有扁平上皮异型性(FEA),1例黏液囊肿样病变(ML)。如果有>2个ADH病灶或<90%的相关钙化被切除,我们建议切除ADH。对于LCIS或ALH患者,如果LCIS或ALH与微钙化相关或LCIS广泛,我们建议切除.当活检<1/2病变时,我们建议切除RS。我们建议所有FEA和ML患者进行6个月的随访。
    结果:根据会议得出的关于切除的共识,切除的27例ADH中,9例升级为浸润性癌或导管原位癌。在建议切除的6例LCIS病例中,没有升级。九个切除的放射状疤痕显示没有升级。此外,3名ADH患者,2与ALH,1与LCIS,2例RS接受了自愿切除,没有升级。所有其他患者(13例ADH,5LCIS,17ALH,22RS,2FEA和1ML)随访成像,在随访期间(187-1389天)均未发现疾病进展的证据。所有11例rad路径不一致病例均被切除,其中2例升级为癌症。
    结论:这项前瞻性研究的结果表明,在建立预定义的坚定指南并进行严格的rad-path相关性后,与观察相比,可以成功地将高风险乳腺病变分类为手术。
    BACKGROUND: The management of high-risk breast lesions diagnosed on image-guided core biopsy remains controversial. We implemented a high-risk breast conference attended by breast pathologists, imagers, and surgeons to prospectively review all contemporary cases in order to provide a consensus recommendation to either surgically excise or follow on imaging at 6-month intervals for a minimum of 2 years.
    METHODS: Between May, 2015 and June, 2019, 127 high-risk lesions were discussed. Of these 127 cases, 116 had concordant radiology-pathology (rad-path) findings. The remaining 11 patients had discordant rad-path findings. Of the 116 concordant cases, 6 were excluded due to lack of the first imaging follow-up until analysis. Of the remaining 110 patients, 43 had atypical ductal hyperplasia (ADH), 12 had lobular carcinoma in situ (LCIS), 19 had atypical lobular hyperplasia (ALH), 33 had radial scar (RS), 2 had flat epithelial atypia (FEA), and 1 had mucocele-like lesion (ML). We recommended excision for ADH if there were > 2 ADH foci or < 90% of the associated calcifications were removed. For patients with LCIS or ALH, we recommended excision if the LCIS or ALH was associated with microcalcifications or the LCIS was extensive. We recommended excision of RS when < 1/2 of the lesion was biopsied. We recommended all patients with FEA and ML for 6-month follow-up.
    RESULTS: Following conference-derived consensus for excision, of the 27 ADH excised, 9 were upgraded to invasive carcinoma or ductal carcinoma in situ. Of the six LCIS cases recommended for excision, none were upgraded. Nine excised radial scars revealed no upgrades. Additionally, 3 patients with ADH, 2 with ALH, 1 with LCIS, and 2 with RS underwent voluntary excision, and none were upgraded. All other patients (13 with ADH, 5 LCIS, 17 ALH, 22 RS, 2 FEA and 1 ML) were followed with imaging, and none revealed evidence of disease progression during follow-up (187-1389 days). All 11 rad-path discordant cases were excised with 2 upgraded to carcinoma.
    CONCLUSIONS: The results of this prospective study indicate that high-risk breast lesions can be successfully triaged to surgery versus observation following establishment of predefined firm guidelines and performance of rigorous rad-path correlation.
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  • 文章类型: Journal Article
    乳腺粘液性病变包括各种良性和恶性上皮突,表现为胞浆内或细胞外粘蛋白,包括粘液样病变,黏液性癌,实性乳头状癌,和其他罕见的产生粘液的癌亚型。最重要的诊断挑战是发现自由漂浮或基质粘蛋白积累,其重要性取决于临床,放射学,和病理背景。本文强调黏液细胞样病变与黏液癌的鉴别诊断,简要考虑了潜在的模仿,如具有粘液样基质(“基质粘蛋白”)和异物的双相和间质病变。
    Mucinous lesions of the breast include a variety of benign and malignant epithelial processes that display intracytoplasmic or extracellular mucin, including mucocelelike lesions, mucinous carcinoma, solid papillary carcinoma, and other rare subtypes of mucin-producing carcinoma. The most important diagnostic challenge is the finding of free-floating or stromal mucin accumulations for which the significance depends on the clinical, radiologic, and pathologic context. This article emphasizes the differential diagnosis between mucocelelike lesions and mucinous carcinoma, with a brief consideration of potential mimics, such as biphasic and mesenchymal lesions with myxoid stroma (\"stromal mucin\") and foreign material.
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  • 文章类型: Journal Article
    Many benign and reactive lesions of the breast show morphological overlap with malignant lesions. These benign mimics of malignancy often present diagnostic challenges to even the most experienced pathologists. This review focuses on several benign lesions of the breast that mimic malignant entities. For each of these lesions, we describe the key morphological and immunohistochemical features, potential diagnostic pitfalls, and our approach to arriving at the correct diagnosis.
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  • 文章类型: Journal Article
    Management of pure mucocele-like lesion (MLL) diagnosed on percutaneous breast biopsy (PBB) is controversial. To assess surgical upgrade rate and clinical outcome of pure MLL obtained as sole diagnosis on PBB. Patients diagnosed with a MLL as the most advanced lesion on PBB from April 1997 to December 2010 were reviewed for radiologic presentation, biopsy technique, and pathologic and clinical outcomes. Of the 21,340 image-guided PBB performed during the study period, 50 women with 51 MLL (0.24%) were identified. Mean age was 53.1 ± 7.7 years. Radiologic findings were mostly microcalcifications (n = 47, 92.2%). Stereotactic PBB was performed for 49 lesions (96.1%). Surgery was performed shortly after biopsy in 35 women, with benign final pathology in 33, and upgrade to ductal carcinoma in situ (DCIS) in two patients (2/35, 5.7%). Mean follow-up was 4.2 ± 2.5 years (3.7 ± 2.1 years for surgical patients; 5.9 ± 2.9 years for follow-up only patients); three women were lost to follow-up (3/50). Three invasive cancers (3/47, 6.4%) were diagnosed 1.2, 1.2, and 2.8 years after biopsy: two in surgical patients, and one in a follow-up only patient. No cancer occurred at the same site as the original MLL. Pure MLL lesion of the breast is a rare entity and is mostly associated with a benign outcome. We observed an upgrade to DCIS slightly superior to 5%, but no invasive cancer. It is therefore unclear if these lesions should be excised or clinically and radiologically followed up when such lesions are found at PBB.
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  • 文章类型: Journal Article
    OBJECTIVE: The purpose of this study was to determine the frequencies of atypia and cancer at excisional biopsy of lesions with a diagnosis of mucocele-like lesion (MLL) at percutaneous breast biopsy.
    METHODS: Retrospective review of 9286 lesions subjected to percutaneous imaging-guided biopsy identified MLLs in 35 (0.38%) patients. Medical records, imaging studies, and histologic results were reviewed.
    RESULTS: Of the 35 patients with core biopsy findings of MLL, 27 underwent stereotactic core needle biopsy (19 with microcalcifications, five with calcifications with an associated mass, and three with only a mass), and eight underwent ultrasound-guided core needle biopsy (four with a solid mass, three with a complex cystic mass). At core biopsy, 12 of 35 (34%) MLLs were associated with atypia (10 cases of atypical ductal hyperplasia, two of flat epithelial atypia), and 23 of 35 (66%) were benign MLL only. All 12 MLLs associated with atypia and 12 of 23 benign MLLs were surgically excised. Eleven patients did not undergo surgery, five of whom were lost to follow-up. One of the 12 (3% of the 35) MLLs associated with atypia was upgraded to DCIS. None were upgraded to invasive cancer. None of the benign MLLs were upgraded to malignancy, and findings at excision of four of the 23 (17%) benign MLLs led to a change in diagnosis to a high-risk lesion (three atypical ductal hyperplasia, one atypical lobular hyperplasia).
    CONCLUSIONS: MLL is a rare diagnosis but is encountered in large-volume breast practices. The findings are nonspecific with a range of imaging appearances. No imaging test is reliable for differentiating MLL from other suspicious lesions or lesions with associated atypia. Surgery is clearly warranted for MLL associated with atypia at core needle biopsy because it may be upgraded to malignancy upon excision. However, if the presence of atypia at excision of benign MLL will change clinical management, then benign MLL at core needle biopsy warrants surgical excision in some cases. In patients whose treatment will not change if atypia is found at excision, close surveillance with short-interval follow-up is a reasonable alternative.
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