Clinical and radiological presentation of pleomorphic lobular carcinoma in-situ and its association with invasive malignancy

Cliona C. Kirwan , Yogesh Jain , Kit Morris , Miles Howe , James R. Harvey
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Abstract

Aims

Optimal management of Pleomorphic lobular carcinoma-in-situ (PLCIS) remains a matter of debate. We aimed to identify presenting clinical, radiological and histopathological features and oncological outcome of PLCIS.

Methods

From a prospectively maintained histopathology database between January 2000 and June 2014, all patients with a diagnosis of PLCIS were identified, and retrospective review of case notes performed.

Results

Of 19 cases, only 3 presented as symptomatic lumps, however 11 had mass lesions on imaging. All patients underwent definitive cancer surgery with wide margins. In all but three cases, PLCIS was associated with additional pathologies (DCIS, ILC, IDC), highlighting the pluripotential development of breast cancer. Of the six cases with no invasion, three were oestrogen receptor negative. There were no local or systemic recurrences over the median follow up period of 66 months.

Conclusion

PLCIS presenting without invasion is rare and, unlike invasive cancer and ductal carcinoma-in-situ, does not appear to be predominantly associated with ER positivity. However, PLCIS is almost universally associated with invasive cancer or DCIS, and should be managed with wide excision and clear margins.

Clinical practise points

  • There is uncertainty surrounding the management of PLCIS as highlighted by the lack of guidelines on this unusual disease entity.

  • The commonest presentation of PLCIS is in asymptomatic women through breast screening.

  • PLCIS presenting without invasion is rare and unlike invasive breast cancer and DCIS, does not appear to be predominantly commonly associated with ER positivity.

  • PLCIS is commonly associated with in-situ and invasive lesions, with 58% of cases associated with invasive lobular carcinoma in this current series.

  • Breast conserving surgery with clear margins and adjuvant treatment as dictated by associated pathology and molecular profile is recommended for PLCIS.

  • In patients presenting with a mass lesion, and pure PLCIS on diagnostic core biopsy: A re-biopsy, ideally using vacuum-assistance is recommended, to attempt to upgrade the tumour pre-operatively, as invasion is almost universal in this subset.

The common association of PLCIS with the presence of invasive ductal carcinoma, invasive lobular carcinoma, ductal carcinoma in-situ and lobular carcinoma-in-situ suggests a single pluripotent stem cell origin for these cancer subtypes.
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多形性小叶原位癌的临床和影像学表现及其与侵袭性恶性肿瘤的关系
目的多形性小叶原位癌(PLCIS)的最佳治疗仍然是一个有争议的问题。我们的目的是确定PLCIS的临床表现、放射学和组织病理学特征以及肿瘤预后。方法从2000年1月至2014年6月期间前瞻性维护的组织病理学数据库中,确定所有诊断为PLCIS的患者,并对病例记录进行回顾性审查。结果19例患者中,仅有3例表现为症状性肿块,11例影像学表现为肿块。所有患者都接受了明确的大切缘肿瘤手术。在除3例外的所有病例中,PLCIS都与其他病理(DCIS、ILC、IDC)相关,突出了乳腺癌的多能性发展。6例无侵袭,3例雌激素受体阴性。在66个月的中位随访期间,没有局部或全身复发。结论plcis表现为无侵袭性是罕见的,与浸润性癌和原位导管癌不同,它并不明显与ER阳性相关。然而,PLCIS几乎普遍与浸润性癌或DCIS相关,应广泛切除和明确边缘。临床实践要点:由于缺乏这种罕见疾病的指南,围绕PLCIS的管理存在不确定性。●最常见的PLCIS表现是无症状的女性通过乳房筛查。●PLCIS表现为无侵袭性是罕见的,与浸润性乳腺癌和DCIS不同,它并不主要与ER阳性相关。●PLCIS通常与原位和浸润性病变相关,在目前的研究中,58%的病例与浸润性小叶癌相关。●根据相关病理和分子特征,建议对PLCIS患者行保乳手术,手术边缘清晰,并进行辅助治疗。●在诊断性核心活检中出现肿块病变和纯PLCIS的患者:建议术前进行再次活检,理想情况下使用真空辅助,以尝试升级肿瘤,因为在该亚群中侵袭几乎是普遍的。PLCIS与浸润性导管癌、浸润性小叶癌、原位导管癌和原位小叶癌的共同关联表明,这些癌症亚型具有单一的多能干细胞起源。
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