Arch Hand Microsurg.  2021 Dec;26(4):265-269. 10.12790/ahm.21.0126.

Malignant Nodular Hidradenoma of the Fingertip: A Case Report

Affiliations
  • 1Department of Plastic and Reconstructive Surgery, Gwangmyeong Sungae General Hospital, Gwangmyeong, Korea
  • 2Department of Pathology, Gwangmyeong Sungae General Hospital, Gwangmyeong, Korea
  • 3Department of Plastic and Reconstructive Surgery, Seoul National University Hospital, Seoul, Korea

Abstract

Malignant nodular hidradenoma (MNH) is an infrequent, highly malignant tumor derived from eccrine sweat glands. MNH usually occurs on the scalp, trunk, and proximal extremities, and rarely on the hand. A 55-year-old male patient visited clinics with a gradually enlarging painless mass at fingertip. It begins a year ago. Recently, it has grown rapidly and starts ulceration, and bleeding over the past 3 weeks. According to the biopsy report, it has focal necrosis, atypia, atypical mitoses, and nuclear pleomorphism suggested that the mass was MNH. After histological diagnosis, tiny bone erosion was observed in the re-read radiographic finding. For the oncologic evaluation, the patient was transferred to the cancer center. Radical amputation was performed to the residual tumor that might remain based on re-reading of radiographs. MNH of the finger is especially difficult to the diagnosis given its rarity and variable histology. When ulcerative skin lesion and radiographic bone erosion are observed, one should suspect malignancy and makes out a proper therapeutic plan after histologic biopsy.

Keyword

Neoplasms; Malignant; Sweat glands; fingers

Figure

  • Fig. 1. A 55-year-old male visited with a 1.5×3.0-cm firm mass. It started 1 year ago and rapidly increased in size from 3 weeks ago with central ulceration and bleeding.

  • Fig. 2. (A) Possibility of hemangioma due to increased vascularity around the mass on ultrasonography. (B) Official reading from the radiologist confirmed that it did not show any unusual findings on magnetic resonance imaging.

  • Fig. 3. During the first operation, the firm solitary mass was removed with the stalk.

  • Fig. 4. (A) Low power view show circumscribed tumor nodule and cystic areas surrounded by a hyaline stroma (H&E stain, ×10). (B) The tumor shows extensive necrosis (asterisks) (H&E stain, ×40). (C) Duct-like structure (empty arrowhead) and cytoplasmic lumen (solid arrowhead) are evident. The tumor cells have pleomorphic and hyperchromatic nuclei (H&E stain, ×400). (D) Mitotic figures (solid arrowhead) are easily found (H&E stain, ×400). Nucleoli are prominent.

  • Fig. 5. (A) No distant metastasis was observed on positron emission tomography-computed tomography. (B, C) Radical amputation was performed due to bone erosive lesions of the distal phalanx found on magnetic resonance imaging re-reading.

  • Fig. 6. No specific complaints and no evidence of metastasis after 1 year.


Reference

1. Souvatzidis P, Sbano P, Mandato F, Fimiani M, Castelli A. Malignant nodular hidradenoma of the skin: report of seven cases. J Eur Acad Dermatol Venereol. 2008; 22:549–54.
Article
2. Chang CH, Chang KP, Huang SH, et al. Hidradenocarcinoma of the fingertip: a case report and literature review. Dermatol Surg. 2011; 37:704–8.
Article
3. Nazerali RS, Tan C, Fung MA, Chen SL, Wong MS. Hidradenocarcinoma of the finger. Ann Plast Surg. 2013; 70:423–6.
Article
4. Kasbekar PU, Shailaja PJ. Case study of a rare case of nodular hidradenoma of the finger. Int J Sci Res. 2013; 3:1–4.
5. Lee JH, Cho SI, Do NY, Dong KW, et al. A case of giant malignant clear cell hidradenoma. Korean J Otolaryngol-Head Neck Surg. 2005; 48:1305–8.
6. Stout AP, Cooley SG. Carcinoma of sweat glands. Cancer. 1951; 4:521–36.
Article
7. Choi BS, Kim YJ, Kim JY, Jo HJ. Nodular hidradenoma on the fourth finger. J Korean Soc Surg Hand. 2013; 18:143–6.
Article
8. Dhawan SS, Nanda VS, Grekin S, Rabinovitz HS. Apocrine adenocarcinoma: case report and review of the literature. J Dermatol Surg Oncol. 1990; 16:468–70.
Article
9. Robson A, Greene J, Ansari N, et al. Eccrine porocarcinoma (malignant eccrine poroma): a clinicopathologic study of 69 cases. Am J Surg Pathol. 2001; 25:710–20.
Full Text Links
  • AHM
Actions
Cited
CITED
export Copy
Close
Share
  • Twitter
  • Facebook
Similar articles
Copyright © 2024 by Korean Association of Medical Journal Editors. All rights reserved.     E-mail: koreamed@kamje.or.kr