• Users Online: 164
  • Home
  • Print this page
  • Email this page
Home About us Editorial board Ahead of print Current issue Search Archives Submit article Instructions Subscribe Contacts Login 


 
 Table of Contents  
CASE REPORT
Year : 2017  |  Volume : 6  |  Issue : 1  |  Page : 11-13

Hidradenocarcinoma presenting with multiple site metastases


Department of Pathology, Maharishi Markandeshwar Institute of Medical Sciences and Research, Ambala, Haryana, India

Date of Web Publication18-Aug-2017

Correspondence Address:
Kriti Chauhan
Department of Pathology, Maharishi Markandeshwar Institute of Medical Sciences and Research, Mullana, Ambala - 133 207, Haryana
India
Login to access the Email id

Source of Support: None, Conflict of Interest: None


DOI: 10.4103/ijhi.ijhi_3_16

Get Permissions

  Abstract 


Hidradenocarcinoma also known as malignant nodular hidradenoma or clear cell hidradenocarcinoma are very uncommon skin adnexal tumors of sweat gland origin known to have a high potential for local reccurence and metastasis. Histologically it is a challenge to diagnose because it very commonly mimics several metastatic visceral malignancies and other non-aggressive skin adnexal tumors. We highlight here the importance of timely diagnosis of hidradenocarcinoma and its differentiation from other look alike because of its poor prognosis and uncertain response to chemotherapy and radiotherapy.

Keywords: Clear cells, hidradenocarcinoma, metastases


How to cite this article:
Chauhan K, Garg M, Dadwal E. Hidradenocarcinoma presenting with multiple site metastases. Int J Histopathol Interpret 2017;6:11-3

How to cite this URL:
Chauhan K, Garg M, Dadwal E. Hidradenocarcinoma presenting with multiple site metastases. Int J Histopathol Interpret [serial online] 2017 [cited 2017 Nov 23];6:11-3. Available from: http://www.ijhi.org/text.asp?2017/6/1/11/213269




  Introduction Top


Hidradenocarcinomas are very rare intradermal malignant tumours of apocrine origin reported to occur on abdomen, trunk, groin, scalp, elbow, eyelid, digits, shoulder and breast.[1],[2],[3] The reported incidence is 0.05%.[3] They have a high metastatic potential, particularly to lymph nodes. Metastases have been reported in more than 60% of patients within first 2 years of diagnosis.[4] We would like to report a case of hidradenocarcinoma presenting with metastasis at multiple sites and discuss the various other tumours (primary and metastatic) from which it should be differentiated as it is quite a challenge to diagnose it correctly on histology.


  Case Report Top


A 55-year-old male patient presented to our institute with an abdominal swelling for 6 months, gradually increasing in size, associated with pain in back and not relieved by medications. On examination, a well-defined lump was noted over the left lumbar region, moving with respiration and fixed to the overlying skin which was otherwise normal. The haematological findings were unremarkable except for a raised total leucocyte count (1200 μ/L). Ultrasound abdomen showed a hypoechoic heterogenous mass measuring 31 mm × 25 mm in the left lower abdominal wall. No organomegaly or any other lesion/tumour was noted. In view of back pain, magnetic resonance imaging spine was done which showed multifocal metastatic deposits in the left paravertebral region at L1–2 level, gluteal region along with enlarged right iliac lymph nodes. Contrast-enhanced computed tomography chest revealed multiple discrete and conglomerate enlarged lymph nodes with areas of necrosis in pretracheal, paraaortic, precarinal, right hilum and bilateral axillary regions. There was an associated lytic destructive lesion in posterior end of the left 4th rib with extrapleural enhancing soft tissue component. Prostate-specific antigen levels were normal (0.57); hence, metastasis from a prostatic carcinoma was ruled out. The liver and renal function tests were unremarkable. This was followed by an excision biopsy of the abdominal wall lump.

Grossly, the lump was skin covered and measured 6.5 cm × 3 cm × 2 cm. On cutting, a well-defined tumour was seen measuring 3 cm × 2.8 cm × 2 cm showing areas of necrosis. The overlying skin was adherent but free of tumour [Figure 1]. Sections were taken from tumour and stained with H and E stain. Microscopy revealed a well-defined tumour in the dermis composed of population of cells showing both squamoid and eccrine differentiation. The cells had well-defined cytoplasmic borders, pale to eosinophilic to abundant clear cytoplasm, vesicular nuclei and prominent nucleoli [Figure 2]. Few duct-like structures were also seen [Figure 3]a. Intervening fibrous septa showed extensive acute inflammatory infiltrate. Numerous typical and atypical mitotic figures along with areas of necrosis were also seen [Figure 3]b. The resection margins were involved. Based on these findings, a diagnosis of hidradenocarcinoma was formed. The clinical tumour node malignant (TNM) stage was T2N2cM1. The patient refused to receive any further treatment having been explained the prognosis and behaviour of tumour and did not turn up for follow-up.
Figure 1: Gross photograph of the tumour and corresponding scanner view showing a tumour in the dermis with no connection to the overlying skin

Click here to view
Figure 2: (a) Low power view showing squamoid morphology of cells (H and E, ×100). (b) Low power view showing tumour cells with eosinophilic cytoplasm (H and E, ×100)

Click here to view
Figure 3: (a) High power view showing gland-like structures (H and E × 400). (b) High power view showing mitotic figures (H and E, ×400)

Click here to view



  Discussion Top


Hidradenocarcinomas are very uncommon intradermal malignant tumours of eccrine origin usually diagnosed in the fifth to seventh decade of life with equal incidence in men and women.[5] Typically, it appears as a benign solitary lesion, but multiple lesions form also has been reported.[2] It presents as an asymptomatic, well-circumscribed nodular lesion that either maintains a stable size or may slowly expand circumferentially.[1] At an undefined period, the tumour transforms into an aggressive form that metastasizes to lymph nodes, bones or visceral organs.[2],[6] It is also known to have a high recurrence rate. It accounts for up to 6% of malignant eccrine tumours and represents the malignant counterpart of hidradenoma. The largest study on malignant sweat gland tumours was done by Berg and McDevitt in 1968 which included a total of 101 cases.[7]

Histopathologically, it is similar to a benign nodular hidradenoma. It comprises epithelial lobules within the dermis showing tubular lamina lined by cuboidal or columnar cells. The solid component is composed of a mixture of eosinophilic polygonal cells, squamous cells and clear cells with distinct boundaries.[2] The cytological features of malignancy include asymmetry, infiltrative growth, lymphovascular invasion, pleomorphism, necrosis and atypical mitotic figures.[1],[8]

The differential diagnosis includes other primary skin tumours with follicular, eccrine or sebaceous differentiation such as adenoid cystic eccrine carcinoma (ACC), aggressive digital papillary adenocarcinoma (ADPA) and cutaneous metastatic diseases from clear cell tumour such as renal cell carcinoma (RCC), thyroid and lung cancers.[2],[9] For example, ACC shows basaloid cells arranged in cribriform or tubular patterns with hyaline material. ADPA shows cystic areas lined by papillary structures. RCC shows clear cell population with intervening prominent vascularization.

In our case, there was no known extracutaneous primary, so any metastasis was ruled out clinically and histologically. The other adnexal tumours were ruled out on the basis of histology. On immunohistochemistry, these tumours stain positive for keratin AE1/3, cytokeratin 5/6, Ki-67 and P53.[10]

Hidradenocarcinoma has a very poor prognosis. The 5 years post-surgical survival rate has been reported to be <30%.[2] The first line of treatment suggested is a surgical excision with at least 2 cm free margin and a selective lymph node dissection.[11] About 50%–60% patients present with local recurrence or metastasis despite complete removal.[12] The role of adjuvant therapy is controversial. Gauerke and Driscoll [1] have suggested that a detailed data including TNM staging, histological type, grade, location and patient age should be taken together to decide an optimal treatment strategy. They have recommended chemotherapy sunitinib (an oral tyrosine kinase inhibitor for metastasis). Radiotherapy is advocated only in few selected cases which exhibit severe histological picture, lymph node invasion or metastasis at the time of diagnosis.[2],[3]


  Conclusion Top


Hidradenocarcinoma is highly aggressive tumours and should be correctly diagnosed. The standard modality of treatment is a wide local excision with clear margins. The histological features are challenging and any metastatic tumour should be first excluded in the study. The role of adjuvant therapy is controversial. An inadequate excision of the lesion appears to be a poor prognostic factor because of a propensity to recur locally. The role of adjuvant therapy is controversial.

Financial support and sponsorship

Nil.

Conflicts of interest

There are no conflicts of interest.



 
  References Top

1.
Gauerke S, Driscoll JJ. Hidradenocarcinomas: A brief review and future directions. Arch Pathol Lab Med 2010;134:781-5.  Back to cited text no. 1
[PUBMED]    
2.
Giorgini E, Tugnoli G, Aprile S, Collina G, Villani S, Biscardi A, et al. Malignant nodular hidradenocarcinoma arising on the areola of a male patient: Case report of an orphan disease and review of the literature. J Carcinog Mutagen 2012;3:129.  Back to cited text no. 2
    
3.
Floros P, Mikhail M. A rare case of pectoral hidradenocarcinoma and brief review. Internet J Surg 2010;26:4.  Back to cited text no. 3
    
4.
Ohta M, Hiramoto M, Fujii M, Togo T. Nodular hidradenocarcinoma on the scalp of a young woman: Case report and review of literature. Dermatol Surg 2004;30:1265-8.  Back to cited text no. 4
[PUBMED]    
5.
Cooper PH. Carcinomas of sweat glands. Pathol Annu 1987;22 Pt 1:83-124.  Back to cited text no. 5
[PUBMED]    
6.
Asati DP, Brahmachari S, Kudligi C, Gupta C. Hidradenocarcinoma: A rare sweat gland neoplasm presenting as small turban tumor of the scalp. Indian J Dermatol 2015;60:421.  Back to cited text no. 6
[PUBMED]  [Full text]  
7.
Berg JW, McDevitt RW. Pathology of sweat gland carcinomas. Pathol Annu 1968;3:123-44.  Back to cited text no. 7
    
8.
Kazakov DV, Ivan D, Kutzner H, Spagnolo DV, Grossmann P, Vanecek T, et al. Cutaneous hidradenocarcinoma: A clinicopathological, immunohistochemical, and molecular biologic study of 14 cases, including Her2/neu gene expression/amplification, TP53 gene mutation analysis, and t(11;19) translocation. Am J Dermatopathol 2009;31:236-47.  Back to cited text no. 8
[PUBMED]    
9.
Volmar KE, Cummings TJ, Wang WH, Creager AJ, Tyler DS, Xie HB. Clear cell hidradenoma: A mimic of metastatic clear cell tumors. Arch Pathol Lab Med 2005;129:e113-6.  Back to cited text no. 9
[PUBMED]    
10.
Ko CJ, Cochran AJ, Eng W, Binder SW. Hidradenocarcinoma: A histological and immunohistochemical study. J Cutan Pathol 2006;33:726-30.  Back to cited text no. 10
[PUBMED]    
11.
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.  Back to cited text no. 11
[PUBMED]    
12.
Garcia-Bonafe MM, Campins MM, Redecilla PH. Malignant nodular hidradenoma on the scalp: Report of a case with fine needle aspiration cytology features and histologic correlation. Acta Cytol 2009;53:576-80.  Back to cited text no. 12
[PUBMED]    


    Figures

  [Figure 1], [Figure 2], [Figure 3]



 

Top
 
 
  Search
 
Similar in PUBMED
   Search Pubmed for
   Search in Google Scholar for
 Related articles
Access Statistics
Email Alert *
Add to My List *
* Registration required (free)

 
  In this article
Abstract
Introduction
Case Report
Discussion
Conclusion
References
Article Figures

 Article Access Statistics
    Viewed154    
    Printed17    
    Emailed0    
    PDF Downloaded42    
    Comments [Add]    

Recommend this journal


[TAG2]
[TAG3]
[TAG4]