Evidence map›Paper›PMID 41732768›Full record

ArticleJPRAS open2026

Sweat gland carcinoma with neuroendocrine differentiation (SCAND) arising in the axilla: A case report highlighting diagnostic challenges and surgical management.

Maiko Inada, Takashi Nouchi, Yoshifumi Iwahashi, Miwako Miyasaka, Yutaka Inaba, Shinichi Asamura

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In one paragraph

Article in JPRAS open, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Maiko InadaDepartment of Plastic and Reconstructive Surgery, Graduate School of Medicine, Wakayama Medical University, Wakayama, Japan.
Takashi NouchiDepartment of Human Pathology and Diagnostic Pathology, Graduate School of Medicine, Wakayama Medical University, Wakayama, Japan.
Yoshifumi IwahashiDepartment of Human Pathology and Diagnostic Pathology, Graduate School of Medicine, Wakayama Medical University, Wakayama, Japan.
Miwako MiyasakaDepartment of Cardiovascular, Respiratory and Breast Surgery, Graduate School of Medicine, Wakayama Medical University, Wakayama, Japan.
Yutaka InabaDepartment of Dermatology, Graduate School of Medicine, Wakayama Medical University, Wakayama, Japan.
Shinichi AsamuraDepartment of Plastic and Reconstructive Surgery, Graduate School of Medicine, Wakayama Medical University, Wakayama, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Sweat gland carcinoma with neuroendocrine differentiation (SCAND) is a rare, newly recognized cutaneous adnexal tumor arising from sweat glands and characterized by neuroendocrine features. Given its rarity and resemblance to benign lesions, clinical diagnosis can be challenging. Case presentation: A 73-year-old man presented with a 40-year history of intermittent discharge from a right axillary mass, which had initially been diagnosed as an epidermal cyst. Following lesion excision along the tumor margin at a local clinic, histopathological analysis revealed apocrine carcinoma, and the surgical margin could not be definitively confirmed to be negative. He was then referred to our department, where positron emission tomography-computed tomography demonstrated abnormal uptake in the right axillary lymph nodes, with a maximum standardized uptake value of 5.70. We performed wide local excision with a 1-cm margin, as well as a level Ⅱ axillary lymph node dissection. Histopathological evaluation showed tumor infiltration with nodular and trabecular pattern in the dermis and the subcutaneous tissue. Tumor cells contained eosinophilic cytoplasm and round-shaped nuclei with granular chromatin. 28 lymph nodes were resected, among which 19 showed metastatic involvement. Immunohistochemistry showed positivity for GCDFP-15, GATA3, ER and neuroendocrine differentiation markers. These findings were consistent with SCAND. The wound was closed primarily without the need for flap reconstruction. There has been no evidence of recurrence or metastasis at 12 months of postoperative follow-up. Conclusion: This case highlights the potential for long-standing benign-appearing skin lesions to harbor rare malignant tumors such as SCAND. Accurate pathological diagnosis and increased clinical awareness among plastic surgeons are essential, and long-term surveillance is recommended owing to the possibility of delayed metastasis.

Indexed as

(LGNECS)Low-grade neuroendocrine carcinoma of the skinSweat gland carcinomaSweat gland carcinoma with neuroendocrine differentiation (SCAND)

Identifiers

PMID41732768
PMCPMC12924892

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