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DOI 10.5021/ad.2014.26.2.177

Медицинская библиотека · Annals of dermatology · 2014

Long-term survival analysis and clinical follow-up in acral lentiginous malignant melanoma undergoing sentinel lymph node biopsy in korean patients.

Jeon Su-Young, Hong Jin-Woo, Lee Suee, Oh Sung Yong, Hong Young-Seoub, Kim Ki-Ho, Song Ki-Hoon

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Аннотация

BACKGROUND

In cutaneous malignant melanoma (MM) with clinically uninvolved regional lymph nodes, sentinel lymph node (SLN) status is the most powerful indicator of both overall survival (OS) and disease-free survival (DFS). However, no studies on the long-term survival and clinical follow-up of Korean patients with acral lentiginous MM (ALM) undergoing SLN biopsy (SLNB) have been published.

OBJECTIVE

The purpose of this study was to investigate the clinical prognosis and long-term survival of Korean patients with ALM according to SLN status.

METHODS

Thirty-four ALM patients undergoing SLNB were included in this study. We evaluated clinical and histopathological follow-up data such as the stage of disease, treatment, recurrence, and metastasis, and analyzed OS and DFS according to SLN status.

RESULTS

The median follow-up time was 60.5 months (range 3~127 months). Positive SLNs were noted in 14 patients (41.2%). Patients with negative SLNs had better OS and DFS than those with positive SLNs (p<0.05). Increased Breslow thickness was associated with short OS and DFS (p<0.05), and female patients showed better DFS than male patients (p<0.05).

CONCLUSION

To our knowledge, this is the first study on the long-term survival and clinical follow-up of patients undergoing SLNB for ALM in Korea. Our findings show that SLN status is an important prognostic factor for predicting OS and DFS.

Для цитирования: Jeon Su-Young, Hong Jin-Woo, Lee Suee, Oh Sung Yong, Hong Young-Seoub, Kim Ki-Ho, Song Ki-Hoon. Long-term survival analysis and clinical follow-up in acral lentiginous malignant melanoma undergoing sentinel lymph node biopsy in korean patients.. Annals of dermatology. 2014. DOI: 10.5021/ad.2014.26.2.177.
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