This article has Open Peer Review reports available.
Metastatic breast carcinoma mimicking a sebaceous gland neoplasm: a case report
© Müller et al; licensee BioMed Central Ltd. 2011
Received: 28 March 2011
Accepted: 2 September 2011
Published: 2 September 2011
Breast cancer is common in women and its metastases involve the skin in approximately one quarter of patients. Accordingly, metastatic breast cancer shown to be cutaneous through histology must be distinguished from a wide variety of other neoplasms as well as the diverse morphologic variants of breast cancer itself.
We report the case of a 61-year-old Caucasian woman with cutaneous metastases of a bilateral ductal breast carcinoma that in histopathological examination mimicked an adnexal neoplasm with sebaceous differentiation.
Against the background of metastatic breast carcinoma, dermatopathological considerations of sebaceous differentiation of skin lesions are presented and discussed focusing on the rare differential diagnosis of sebaceous carcinoma of the breast.
Skin metastases of malignant tumors arise principally when the diagnosis of the primary cancer has been previously established, and cutaneous metastases from internal malignancies are an infrequent, although not totally rare, phenomenon . In contrast, breast cancer is very common in women and its metastases frequently involve skin, with cutaneous findings in about one quarter of breast cancer patients .
Cutaneous metastases of carcinomas are encountered in 0.7-9.0% of all patients with cancer in general . In the main, skin metastases occur long after the diagnosis of cancer, however, in some cases they may be the first sign of clinically silent visceral malignancies. The location of skin metastases depends on the location of the primary malignancy, the mechanism of the metastatic spread, and the gender of the patient. Cutaneous metastases can vary in size and clinical appearance dependent upon the type of primary malignancy. Some skin metastases may mimic benign dermatological conditions such as cutaneous cysts, hemangiomata, herpes zoster eruptions, alopecic patches, and erysipelas .
In 2010 Fernandez-Flores investigated 78 cutaneous biopsies from 69 patients and identified six histological patterns of cutaneous metastasis: nodular, diffuse, infiltrative, intravascular, bottom heavy, and top heavy . The majority of the patients were between 60 and 80 years of age. The most frequent anatomical location of the metastases was the abdomen. As to the primary tumor, breast carcinoma was the most common in females. In 18% the origin of the primary tumor was unknown and in all the cases investigated there had been no clinical suspicion of metastasis .
In breast carcinoma in particular there is a wide range of clinical presentation of skin metastases. Most metastases are observed on the chest wall; less common sites include scalp, neck, upper extremities, abdomen and back . In general, eight specific clinical patterns associated with cutaneous breast cancer are known: cancer en cuirasse , inflammatory metastatic carcinoma (carcinoma erysipelatodes) [2, 5], carcinoma teleangiectaticum [4, 6], alopecia neoplastica [7, 8], Paget's disease [9, 10], breast carcinoma of the inframammary crease , metastatic mammary carcinoma of the eyelid with histiocytoid histology , nodular metastases [13, 14], and mucinous adenocarcinoma metastatic to the skin . Skin metastases from breast carcinoma can also be present in a zosteriform distribution when occurring at the sides of the abdomen [13, 15]. Metastatic nodules are primarily caused by hematogenous spread, whereas inflammatory carcinomas and carcinoma en cuirasse are caused by lymphatic spread . In a case of cancer en cuirasse the fibrotic response is induced by the invading cancer with infiltrating tumor cells that resemble single files . This leads to the formation of a chest wall that resembles a metal breastplate of a cuirassier (a mounted cavalry soldier) [2, 4]. In a case of Paget's disease, tumor cells infiltrate the epidermis directly with a typical pagetoid spreading [7, 16]. Alopecia neoplastica presents as oval plaques or patches on the scalp that may be confused clinically with alopecia areata [7, 16]. Breast carcinoma metastases of the scalp usually manifest as cutaneous nodules, although they also manifest less commonly as alopecia neoplastica.
Tracking the differentiation from primary cutaneous malignancies can be challenging due to the ability of the tumor cells to mimic specific dermal structures. Although most skin metastases show morphologic and immunohistologic features of the primary malignancy, they can also mimic other dermatological patterns on histology.
Further examination of our patient was then initiated. It showed a second moderately differentiated invasive ductal breast carcinoma of her right breast with a sonographic tumor thickness of 5 mm (Figure 1, left). Computed chest tomography revealed multiple pulmonary and lymphatic metastatic lesions within the ipsilateral axillary lymph nodes. This ductal breast carcinoma was positive for ER and PR. Ki67 expression demonstrated that 20% of the tumor cells were proliferating. No overexpression of HER-2/neu was observed.
Synopsis of disease
Five years prior to presentation
Poorly differentiated invasive solid ductal breast carcinoma of the left breast.
ER positive (60%);
PR positive (70%);
Ablatio mammae left.
Axillary lymph node dissection left.
Radiochemotherapy with paclitaxel.
No organ metastasis
Metastatic breast cancer of the scalp with the histologic appearance of a sebaceously differentiated primary cutaneous carcinoma of the scalp.
ER and PR positive;
Pulmonary and lymph node metastases.
Two month after presentation
Moderately differentiated invasive solid ductal breast carcinoma of her left mammary.
ER positive (30%);
PR positive (> 90%);
Ablatio mammae right with sentinel node biopsy right.
Chemotherapy with paclitaxel and bevacizumab.
We were able to establish the final diagnosis of metastatic breast cancer with the histologic appearance of a sebaceous differentiated primary cutaneous carcinoma. Our patient had bilateral ductal breast cancer with identical hormone receptor status within five years. It remains unclear whether the cutaneous metastasis originated from the initially diagnosed breast cancer of her left mammary or from the second ductal carcinoma of her right breast.
Cutaneous metastatic breast cancer must be distinguished from a wide variety of other neoplasms using histology. In the case presented, the tumor cells imitated the histological and immunohistological pattern of a sebaceous gland neoplasm.
Interestingly, sebaceous differentiation can also occur in variable morphologic types of breast carcinoma, such as infiltrating or invasive ductal carcinoma, adenoid cystic carcinoma as well as others . It was therefore critical to determine whether the breast carcinoma of our patient showed any differentiation towards sebaceous carcinoma of the breast within a ductal mammary carcinoma. In this setting, a dermatopathologist must also bear in mind the differential diagnosis of an underlying metastasizing carcinoma of the breast with sebaceous differentiation (synonymous with sebaceous carcinoma of the breast) .
The first description of a mammary sebaceous carcinoma was made in 1977 as a variant of lipid-rich carcinoma of the mammary gland . The immunoreactivity is similar to other previously described sebaceous carcinomas (cytokeratin, EMA and CEA). Contradictory opinions exist concerning the immunohistochemistry for the androgen receptor, ER and PR . Additionally, controversy remains as to whether sebaceous carcinoma of the breast is a distinct entity or a variant of lipid-rich carcinoma of the breast . Hence, little is known about the prognosis of sebaceous carcinoma of the breast in general .
Regardless of this histogenetic discussion, dermatopathologists must be aware of this opportunity for misdiagnosis of diverse sebaceous neoplasms of the skin. Histological mimicry can hamper the correct diagnosis in small biopsy specimens because the lesions cannot be evaluated as whole, dimensional structures. Therefore, suspicious lesions should be excised completely. Reactivity for adipophilin is of great advantage in this setting . Adipophilin was recently shown to be expressed in sebocytes and sebaceous lesions and can be valuable in an immunohistochemical panel when evaluating cutaneous lesions with clear cell histology in order to differentiate true sebaceous origin from its epigones, as in this case.
Clinically, our patient presented with a reddish nodule on her scalp that caused focal alopecia, which was misdiagnosed in the first biopsy specimen as primary carcinoma of the skin with sebaceous differentiation. Due to the uncommon differentiation of the cells and the sebaceous-like pattern, diagnosis of cutaneous metastasis of a breast carcinoma was hard to establish on the biopsy. Only after complete removal of the lesion and with knowledge of the whole history of our patient could we finally establish the diagnosis of metastatic breast cancer.
Written informed consent for publication from the patient's next of kin could not be obtained despite all reasonable attempts. The case is important to public health and every effort has been made to protect the identity of our patient. There is no reason to believe that our patient would object to publication.
- Fernandez-Flores A: Cutaneous metastases: a study of 78 biopsies from 69 patients. Am J Dermatopathol. 2010, 32 (3): 222-239.PubMedGoogle Scholar
- Schwartz RA, Rothenberg J: Metastatic adenocarcinoma of breast within a benign melanocytic nevus in the context of cutaneous breast metastatic disease. J Cutan Pathol. 2010, 37 (12): 1251-1254. 10.1111/j.1600-0560.2009.01480.x.View ArticlePubMedGoogle Scholar
- Hussein MR: Skin metastasis: a pathologist's perspective. J Cutan Pathol. 2010, 37 (9): e1-20. 10.1111/j.1600-0560.2009.01469.x.View ArticlePubMedGoogle Scholar
- Lin JH, Lee JY, Chao SC, Tsao CJ: Telangiectatic metastatic breast carcinoma preceded by en cuirasse metastatic breast carcinoma. Br J Dermatol. 2004, 151 (2): 523-524. 10.1111/j.1365-2133.2004.06140.x.View ArticlePubMedGoogle Scholar
- Marneros AG, Blanco F, Husain S, Silvers DN, Grossman ME: Classification of cutaneous intravascular breast cancer metastases based on immunolabeling for blood and lymph vessels. J Am Acad Dermatol. 2009, 60 (4): 633-638. 10.1016/j.jaad.2008.11.008.View ArticlePubMedGoogle Scholar
- Dobson CM, Tagor V, Myint AS, Memon A: Telangiectatic metastatic breast carcinoma in face and scalp mimicking cutaneous angiosarcoma. J Am Acad Dermatol. 2003, 48 (4): 635-636. 10.1067/mjd.2003.256.View ArticlePubMedGoogle Scholar
- Conner KB, Cohen PR: Cutaneous metastasis of breast carcinoma presenting as alopecia neoplastica. South Med J. 2009, 102 (4): 385-389. 10.1097/SMJ.0b013e31819b0c26.View ArticlePubMedGoogle Scholar
- Haas N, Hauptmann S: Alopecia neoplastica due to metastatic breast carcinoma vs. extramammary Paget's disease: mimicry in epidermotropic carcinoma. J Eur Acad Dermatol Venereol. 2004, 18 (6): 708-710. 10.1111/j.1468-3083.2004.01034.x.View ArticlePubMedGoogle Scholar
- Kao GF, Graham JH, Helwig EB: Paget's disease of the ectopic breast with an underlying intraductal carcinoma: report of a case. J Cutan Pathol. 1986, 13 (1): 59-66. 10.1111/j.1600-0560.1986.tb00461.x.View ArticlePubMedGoogle Scholar
- Petersson F, Ivan D, Kazakov DV, Michal M, Prieto VG: Pigmented Paget disease--a diagnostic pitfall mimicking melanoma. Am J Dermatopathol. 2009, 31 (3): 223-226. 10.1097/DAD.0b013e3181930dc6.View ArticlePubMedGoogle Scholar
- Sanki A, Spillane A: Diagnostic and treatment challenges of inframammary crease breast carcinomas. ANZ J Surg. 2006, 76 (4): 230-233. 10.1111/j.1445-2197.2006.03694.x.View ArticlePubMedGoogle Scholar
- Hood CI, Font RL, Zimmerman LE: Metastatic mammary carcinoma in the eyelid with histiocytoid appearance. Cancer. 1973, 31 (4): 793-800. 10.1002/1097-0142(197304)31:4<793::AID-CNCR2820310406>3.0.CO;2-A.View ArticlePubMedGoogle Scholar
- Bassioukas K, Nakuci M, Dimou S, Kanellopoulou M, Alexis I: Zosteriform cutaneous metastases from breast adenocarcinoma. J Eur Acad Dermatol Venereol. 2005, 19 (5): 593-596. 10.1111/j.1468-3083.2005.01205.x.View ArticlePubMedGoogle Scholar
- Torchia D, Palleschi GM, Terranova M, Antiga E, Melani L, Caproni M, Fabbri P: Ulcerative carcinoma of the breast with zosteriform skin metastases. Breast J. 2006, 12 (4): 385.-10.1111/j.1075-122X.2006.00285.x.View ArticlePubMedGoogle Scholar
- Al Zouman A, Al Harthi F: Male breast carcinoma with zosteriform metastasis. Breast J. 2010, 16 (1): 88-89. 10.1111/j.1524-4741.2009.00826.x.View ArticlePubMedGoogle Scholar
- Baum EM, Omura EF, Payne RR, Little WP: Alopecia neoplastica--a rare form of cutaneous metastasis. J Am Acad Dermatol. 1981, 4 (6): 688-694. 10.1016/S0190-9622(81)80201-0.View ArticlePubMedGoogle Scholar
- Hisaoka M, Takamatsu Y, Hirano Y, Maeda H, Hamada T: Sebaceous carcinoma of the breast: case report and review of the literature. Virchows Arch. 2006, 449 (4): 484-488. 10.1007/s00428-006-0264-8.View ArticlePubMedGoogle Scholar
- van Bogaert LJ, Maldague P: Histologic variants of lipid-secreting carcinoma of the breast. Virchows Arch A Pathol Anat Histol. 1977, 375 (4): 345-353. 10.1007/BF00427064.View ArticlePubMedGoogle Scholar
- Murakami A, Kawachi K, Sasaki T, Ishikawa T, Nagashima Y, Nozawa A: Sebaceous carcinoma of the breast. Pathol Int. 2009, 59 (3): 188-192. 10.1111/j.1440-1827.2009.02349.x.View ArticlePubMedGoogle Scholar
- Ostler DA, Prieto VG, Reed JA, Deavers MT, Lazar AJ, Ivan D: Adipophilin expression in sebaceous tumors and other cutaneous lesions with clear cell histology: an immunohistochemical study of 117 cases. Mod Pathol. 2010, 23 (4): 567-573. 10.1038/modpathol.2010.1.View ArticlePubMedGoogle Scholar
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.