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1.
Autops. Case Rep ; 10(1): 2019115, Jan.-Mar. 2020. ilus
Artículo en Inglés | LILACS | ID: biblio-1087653

RESUMEN

Tailgut cysts (TGCs) are rare congenital entities arising from remnants of the embryological postanal primitive gut. Malignancy in TGCs is rare, with the majority being adenocarcinomas and carcinoid tumors. A search of the published literature yielded only 27 cases of adenocarcinoma developing in TGCs. We described the case of a 54-year-old female who presented with complaints of pelvic and perineal pain of several weeks. After the initial work-up, a mass in the right presacral location was diagnosed. She underwent radical resection of the tumor, using a posterior approach. The lesion was removed en bloc with the middle rectum, coccyx, and sacrum (S4­S5). The histopathologic examination revealed an adenocarcinoma arising in a TGC, and the patient received adjuvant chemoradiotherapy. Our case underlines that diagnosing a TGC is difficult as it is a rare congenital lesion. Clinical examination may be challenging as TGCs present with various symptoms, which can mimic other commonly proctologic disorders. Patients should be referred to a tertiary center with experience in pelvic surgery and must be managed by a multidisciplinary approach to maximize successful treatment. The recommended treatment is surgical excision given the malignant potential of TGCs and their risk of causing local complications.


Asunto(s)
Humanos , Femenino , Persona de Mediana Edad , Neoplasias Pélvicas , Quistes/cirugía , Quistes/diagnóstico , Anomalías Congénitas , Adenocarcinoma
2.
Autops. Case Rep ; 9(4): e2019116, Oct.-Dec. 2019. ilus
Artículo en Inglés | LILACS | ID: biblio-1024253

RESUMEN

Basal cell carcinoma (BCC) is the most common skin cancer. It generally has an indolent course with low rates of metastasis and mortality. However, BCC is locally invasive and can cause significant morbidity due to destructive local spread. We report our experience with a patient who was referred to our skin cancer unit due to a previously neglected lesion on the parietal region of the scalp, which had developed for 7 years. The patient was prescribed vismodegib on the basis that surgery could cause excessive functional and aesthetic damage. The patient had an objective partial response after 20 months of treatment. He was then submitted to radical skin excision, leaving a large defect that was reconstructed using a free latissimus dorsi muscle flap. The patient recovered well, and at the 1-year follow-up there were no signs of local recurrence. Our case demonstrates the value of vismodegib treatment prior to surgery in a locally advanced, high-risk scalp BCC and highlights the importance of an individualized and specialized approach with these patients, within a multidisciplinary team.


Asunto(s)
Humanos , Masculino , Persona de Mediana Edad , Carcinoma Basocelular/tratamiento farmacológico , Neoplasias de Cabeza y Cuello/patología , Grupo de Atención al Paciente , Procedimientos de Cirugía Plástica , Terapia Neoadyuvante , Antineoplásicos/uso terapéutico
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