Tajiri Wakako, Shimamoto Ryo, Koga Yutaka, Kawasaki Junji, Higuchi Makiko, Nakamura Yoshiaki, Koi Yumiko, Koga Chinami, Ijichi Hideki, Choi Ilseung, Suehiro Youko, Taguchi Kenichi, Tokunaga Eriko
Department of Breast Oncology, National Organization Kyushu Cancer Center, 3-1-1 Notame, Minami-Ku, Fukuoka, 811-1395, Japan.
Department of Plastic Surgery, National Organization Kyushu Cancer Center, 3-1-1 Notame, Minami-Ku, Fukuoka, 811-1395, Japan.
Surg Case Rep. 2024 Aug 23;10(1):196. doi: 10.1186/s40792-024-01996-6.
Breast implant-associated anaplastic large-cell lymphoma (BIA-ALCL) is a rare malignancy. Many cases of BIA-ALCL are identified based on the presence of late-onset effusion and/or masses. Importantly, the United States Food and Drug Administration noted that in all cases diagnosed in patients with textured implants, the patients either had a history of mixed implantation of smooth and textured devices or no clinical history was supplied for review. In Japan, the first case of BIA-ALCL was reported in 2019, and we encountered the third case in Japan in December 2021. There have been a total of five cases of BIA-ALCL previously reported at Japanese academic conferences (Japan Oncoplastic Breast Surgery Society. http://jopbs.umin.jp/medical/index.html ), of which only the first case has been published. Unlike the first case, this patient had clinical features that were highly suggestive of the postoperative chest wall recurrence of breast cancer, with a mass and rash on the skin.
The patient was a 45-year-old woman who had undergone breast reconstruction after breast cancer surgery of the right breast 8 years previously. The patient presented with a mass and skin rash inside the inframammary area, and we suspected a damaged silicone breast implant (SBI) or chest wall recurrence. We examined the mass by a core needle biopsy and made a pathological diagnosis of BIA-ALCL. Imaging findings suggested internal thoracic lymph node swelling and lymphoma infiltration beyond the capsule but no metastatic lesions (cStage III). After en bloc resection of the SBI and lymphoma, adjuvant systemic therapy was performed.
We encountered the third case of BIA-ALCL in Japan. This was a case with clinically advanced stage of disease; however, the BIA-ALCL was found to be in remission.
乳房植入物相关间变性大细胞淋巴瘤(BIA-ALCL)是一种罕见的恶性肿瘤。许多BIA-ALCL病例是根据迟发性积液和/或肿块的存在而确诊的。重要的是,美国食品药品监督管理局指出,在所有诊断为有纹理植入物患者的病例中,患者要么有光滑和有纹理装置混合植入史,要么没有提供临床病史以供审查。在日本,2019年报告了首例BIA-ALCL病例,我们于2021年12月在日本遇到了第三例。此前在日本学术会议(日本肿瘤整形乳房外科学会。http://jopbs.umin.jp/medical/index.html )上共报告了5例BIA-ALCL病例,其中只有首例已发表。与首例不同,该患者具有高度提示乳腺癌术后胸壁复发的临床特征,皮肤有肿块和皮疹。
患者为一名45岁女性,8年前因右乳乳腺癌手术接受了乳房重建。患者在乳房下区域出现肿块和皮疹,我们怀疑是硅胶乳房植入物(SBI)受损或胸壁复发。我们通过粗针活检检查了肿块,并做出了BIA-ALCL的病理诊断。影像学检查结果提示胸内淋巴结肿大和淋巴瘤包膜外浸润,但无转移病灶(临床分期III期)。在整块切除SBI和淋巴瘤后,进行了辅助全身治疗。
我们在日本遇到了第三例BIA-ALCL病例。这是一例临床疾病晚期的病例;然而,发现BIA-ALCL已缓解。