Bratiloveanu Miruna, Dumitru Mihai, Marinescu Andreea Nicoleta, Serboiu Crenguta, Patrascu Oana Maria, Costache Adrian, Vrinceanu Daniela
Pathology Department, Carol Davila University of Medicine and Pharmacy, 050474 Bucharest, Romania.
ENT Department, Carol Davila University of Medicine and Pharmacy, 050751 Bucharest, Romania.
Medicina (Kaunas). 2024 Dec 29;61(1):37. doi: 10.3390/medicina61010037.
: Carcinoma ex-pleiomorphic adenoma (CXPA) is a carcinoma derived from a primary or recurrent pleiomorphic adenoma. Microscopically, non-invasive CXPA (intracapsular and carcinoma in situ), minimally invasive CXPA (extracapsular invasion less than 1.5 mm), and invasive CXPA (extracapsular invasion more than 1.5 mm) are described. We performed a retrospective clinical study over the period of 2009-2023 in patients admitted to the ENT Department of the Bucharest University Emergency Hospital. In the studied group, there was a net male predominance of 2.5:1. The tumor evolution until presentation was 6.64 years on average, with values between 2 and 20 years. The reasons for presenting to our department included a sudden increase in size in eleven cases (78.57%), pain in nine cases (64.29%), peripheral facial paralysis in eight cases (57.14%), skin invasion/ulceration in five cases (35.71%), and massive tumor hemorrhage in one case (7.14%). There were histopathological results on paraffin of myoepithelial CXPA in four cases (28.57%), of high-grade CXPA (salivary duct, secretory) in eight cases (57.14%), and of squamous CXPA in two cases (14.29%). The patients with unfavorable evolution showed the following characteristics: a tumor diameter over 11 cm (four cases), integument invasion (four cases), perivascular invasion at HP exam (six cases), perineural invasion at HP exam (six cases), and invasion of the ganglion (three N3b cases and two N1 cases). CXPA is a neoplasia that, when associated with large tumor volumes or peripheral facial paralysis in particular, is a challenge for both the doctor and patient.
多形性腺瘤恶变(CXPA)是一种源自原发性或复发性多形性腺瘤的癌。在显微镜下,可分为非侵袭性CXPA(囊内型和原位癌)、微侵袭性CXPA(囊外侵犯小于1.5毫米)和侵袭性CXPA(囊外侵犯大于1.5毫米)。我们对2009年至2023年期间在布加勒斯特大学急诊医院耳鼻喉科住院的患者进行了一项回顾性临床研究。在研究组中,男性与女性的比例为2.5:1。肿瘤发展至就诊时的平均时间为6.64年,范围在2至20年之间。患者前来我科就诊的原因包括:11例(78.57%)肿瘤大小突然增大、9例(64.29%)疼痛、8例(57.14%)周围性面瘫、5例(35.71%)皮肤侵犯/溃疡以及1例(7.14%)肿瘤大量出血。4例(28.57%)患者的石蜡切片有肌上皮CXPA的组织病理学结果,8例(57.14%)有高级别CXPA(涎腺导管癌、分泌型)的组织病理学结果,2例(14.29%)有鳞状CXPA 的组织病理学结果。病情发展不利的患者具有以下特征:肿瘤直径超过11厘米(4例)、累及皮肤(4例)、组织病理学检查显示血管周围侵犯(6例)、组织病理学检查显示神经周围侵犯(6例)以及神经节侵犯(3例N3b病例和2例N1病例)。CXPA是一种肿瘤,尤其是当它与大体积肿瘤或周围性面瘫相关时,对医生和患者来说都是一项挑战。