Introduction: Breast Implant-Associated Anaplastic Large Cell Lymphoma (BIA-ALCL) is a rare T-cell lymphoma occurring after breast implant procedures. As gender confirmation therapy (GCT) in male-to-female transgender (FT), up to 60–70 % of patients require breast augmentation and are at risk for BIA-ALCL. Hence, we report the youngest BIA-ALCL case in the Italian population and the first early-stage BIA-ALCL occurred in FT patients. Case presentation: A 27-years-old FT was admitted to outpatients' clinics due to swollen left breast. The patient underwent GCT with a macrotextured implant four years before. Clinical examination revealed swollen left breast. Ultrasound and magnetic resonance imaging confirmed left breast periprosthetic effusion. Positron emission tomography-computed tomography scan did not reveal any focal pathological uptake. Fine needle aspiration cytology confirmed BIA-ALCL suspect. The patient underwent bilateral en bloc breast implant removal and periprosthetic capsulectomy. Due to the early stage, adjuvant chemotherapy was omitted. Postoperative follow-up was unremarkable. Clinical discussion: BIA-ALCL is a rare, emergent clinical concern after breast implant surgery. GCT leads to improved body satisfaction and quality of life in FT individuals. As for non-trans patients undergoing breast reconstruction or breast augmentation, this clinical case once again demonstrates that FT patients undergoing breast implant surgery are at risk of BIA-ALCL. Conclusion: Physicians should promote awareness among patients' GCT and tailored postoperative follow-up.

Materazzo, M., Vanni, G., Rho, M., Buonomo, C., Morra, E., Mori, S. (2022). Breast implant-associated anaplastic large cell lymphoma (BIA-ALCL) in a young transgender woman: a case report. INTERNATIONAL JOURNAL OF SURGERY CASE REPORTS, 98 [10.1016/j.ijscr.2022.107520].

Breast implant-associated anaplastic large cell lymphoma (BIA-ALCL) in a young transgender woman: a case report

Materazzo, M.;Vanni, G.;Rho, M.;Buonomo, C.;Mori, S.
2022-01-01

Abstract

Introduction: Breast Implant-Associated Anaplastic Large Cell Lymphoma (BIA-ALCL) is a rare T-cell lymphoma occurring after breast implant procedures. As gender confirmation therapy (GCT) in male-to-female transgender (FT), up to 60–70 % of patients require breast augmentation and are at risk for BIA-ALCL. Hence, we report the youngest BIA-ALCL case in the Italian population and the first early-stage BIA-ALCL occurred in FT patients. Case presentation: A 27-years-old FT was admitted to outpatients' clinics due to swollen left breast. The patient underwent GCT with a macrotextured implant four years before. Clinical examination revealed swollen left breast. Ultrasound and magnetic resonance imaging confirmed left breast periprosthetic effusion. Positron emission tomography-computed tomography scan did not reveal any focal pathological uptake. Fine needle aspiration cytology confirmed BIA-ALCL suspect. The patient underwent bilateral en bloc breast implant removal and periprosthetic capsulectomy. Due to the early stage, adjuvant chemotherapy was omitted. Postoperative follow-up was unremarkable. Clinical discussion: BIA-ALCL is a rare, emergent clinical concern after breast implant surgery. GCT leads to improved body satisfaction and quality of life in FT individuals. As for non-trans patients undergoing breast reconstruction or breast augmentation, this clinical case once again demonstrates that FT patients undergoing breast implant surgery are at risk of BIA-ALCL. Conclusion: Physicians should promote awareness among patients' GCT and tailored postoperative follow-up.
2022
Pubblicato
Rilevanza internazionale
Articolo
Esperti anonimi
Settore MEDS-06/A - Chirurgia generale
English
BIA-ALCL
Breast implants
Breast neoplasm
Lymphoma, large-cell, anaplastic
Transgender persons
Materazzo, M., Vanni, G., Rho, M., Buonomo, C., Morra, E., Mori, S. (2022). Breast implant-associated anaplastic large cell lymphoma (BIA-ALCL) in a young transgender woman: a case report. INTERNATIONAL JOURNAL OF SURGERY CASE REPORTS, 98 [10.1016/j.ijscr.2022.107520].
Materazzo, M; Vanni, G; Rho, M; Buonomo, C; Morra, E; Mori, S
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2108/394010
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