We report a 52-year-old woman who presented with a painless mobile nodule of the axilla of unknown duration. The physical examination found a small, mobile, painless and circumscribed nodule of the axilla. There was no associated regional lymphadenopathy. The patient had a simple excision of the nodule. Gross examination revealed a well-circumscribed nodule measuring 1 cm of diameter. Histologically, the tumor was composed of lobules of well-differentiated dilated tubular structures situated in the dermis and the subcutis (Figs. <xref ref-type="fig" rid="F1">1</xref> and <xref ref-type="fig" rid="F2">2</xref>). The tubules were double-lined by an inner layer of typical apocrine epithelial cells and an outer layer of myoepithelial cells (<xref ref-type="fig" rid="F3">Fig. 3</xref>). A focal ductal differentiation was noted. The intervening stroma was scanty and fibrous with minimal inflammatory cells (<xref ref-type="fig" rid="F1">Fig. 1</xref>). There was no evidence of comedolike channels, hyaline, or clear cell differentiation. The diagnosis of tubular apocrine adenoma was retained. The patient received no further therapy and was well during the 3 months period after excision. <fig id="F1"> <label>Figure 1</label> <caption> Lobules of well-differentiated dilated tubular structures situated in the dermis and separated by a scanty fibrous stroma </caption> <graphic xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="OURD-6-360-g001.tif"/> </fig> <fig id="F2"> <label>Figure 2</label> <caption> The tubules structures reach the subcutis </caption> <graphic xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="OURD-6-360-g002.tif"/> </fig> <fig id="F3"> <label>Figure 3</label> <caption> The tubules are double-lined by an inner layer of apocrine cells and an outer layer of myoepithelial cells </caption> <graphic xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="OURD-6-360-g003.tif"/> </fig> Prior to the study, patient gave written consent to the examination and biopsy after having been informed about the procedure. Tubular apocrine adenoma also called apocrine adenoma, tubulopapillary hidradenoma and papillary tubular adenoma is a rare benign tumor. It predominates in women with a sex ratio of 2:1. The wide age distribution ranges between 18 and 78 years. The scalp is most commonly affected although lesions have been described at a variety of other sites including the face, eyelid, axilla, leg, and genitalia. In the scalp, lesions often arise in a background of nevus sebaceus and may be associated with syringocystadenoma papilliferum. Clinically, the tumor generally presents as a dermal nodule 1–2 cm in diameter or pedunculated lesion, frequently of many years duration. Histologically, tubular apocrine adenoma presents most often as lobules of well-differentiated tubular structures located in the dermis and sometimes the subcutis. The tubules are lined by an inner layer of tall columnar cells, which show decapitation secretion, and frequently show an outer layer of cuboidal cells. Comedo-like channels that extend into the epidermis and connect with some of the tubular structures are occasionally seen. The stroma is composed of fibrous tissue with few inflammatory cells. This is in contrast to syringocystadenoma papilliferum, which contains numerous inflammatory cells in the stroma. The tubular adenoma is benign and recurrence following excision is uncommon. </sec> <sec id="sec1-2"> <title>CONSENT

OURD

Our Dermatol Online

2081-9390

Our Dermatology Online

Poland

OURD-6-360

10.7241/ourd.20153.97

Clinical Image

Tubular apocrine adenoma of the axilla: A rare adnexal tumor

Attafi

Salsabil

Smichi

Ines

Rkik

Wafa

Pathology Department of Siliana Hospital, Siliana, Tunis, Tunisia

Corresponding author: Dr. Salsabil Attafi, E-mail: sehlisalsabil@hotmail.com

2015

6 3 360 361 04012015 11032015

2015

This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

We report a 52-year-old woman who presented with a painless mobile nodule of the axilla of unknown duration. The physical examination found a small, mobile, painless and circumscribed nodule of the axilla. There was no associated regional lymphadenopathy. The patient had a simple excision of the nodule. Gross examination revealed a well-circumscribed nodule measuring 1 cm of diameter. Histologically, the tumor was composed of lobules of well-differentiated dilated tubular structures situated in the dermis and the subcutis (Figs. <xref ref-type="fig" rid="F1">1</xref> and <xref ref-type="fig" rid="F2">2</xref>). The tubules were double-lined by an inner layer of typical apocrine epithelial cells and an outer layer of myoepithelial cells (<xref ref-type="fig" rid="F3">Fig. 3</xref>). A focal ductal differentiation was noted. The intervening stroma was scanty and fibrous with minimal inflammatory cells (<xref ref-type="fig" rid="F1">Fig. 1</xref>). There was no evidence of comedolike channels, hyaline, or clear cell differentiation. The diagnosis of tubular apocrine adenoma was retained. The patient received no further therapy and was well during the 3 months period after excision. <fig id="F1"> <label>Figure 1</label> <caption> Lobules of well-differentiated dilated tubular structures situated in the dermis and separated by a scanty fibrous stroma </caption> <graphic xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="OURD-6-360-g001.tif"/> </fig> <fig id="F2"> <label>Figure 2</label> <caption> The tubules structures reach the subcutis </caption> <graphic xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="OURD-6-360-g002.tif"/> </fig> <fig id="F3"> <label>Figure 3</label> <caption> The tubules are double-lined by an inner layer of apocrine cells and an outer layer of myoepithelial cells </caption> <graphic xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="OURD-6-360-g003.tif"/> </fig> Prior to the study, patient gave written consent to the examination and biopsy after having been informed about the procedure. Tubular apocrine adenoma also called apocrine adenoma, tubulopapillary hidradenoma and papillary tubular adenoma is a rare benign tumor. It predominates in women with a sex ratio of 2:1. The wide age distribution ranges between 18 and 78 years. The scalp is most commonly affected although lesions have been described at a variety of other sites including the face, eyelid, axilla, leg, and genitalia. In the scalp, lesions often arise in a background of nevus sebaceus and may be associated with syringocystadenoma papilliferum. Clinically, the tumor generally presents as a dermal nodule 1–2 cm in diameter or pedunculated lesion, frequently of many years duration. Histologically, tubular apocrine adenoma presents most often as lobules of well-differentiated tubular structures located in the dermis and sometimes the subcutis. The tubules are lined by an inner layer of tall columnar cells, which show decapitation secretion, and frequently show an outer layer of cuboidal cells. Comedo-like channels that extend into the epidermis and connect with some of the tubular structures are occasionally seen. The stroma is composed of fibrous tissue with few inflammatory cells. This is in contrast to syringocystadenoma papilliferum, which contains numerous inflammatory cells in the stroma. The tubular adenoma is benign and recurrence following excision is uncommon. </sec> <sec id="sec1-2"> <title>CONSENT

The examination of the patient was conducted according to the Declaration of Helsinki principles.

Source of Support: Nil,

Conflict of Interest: None declared.