Journal of Indian Association of Pediatric Surgeons
Journal of Indian Association of Pediatric Surgeons
                                                   Official journal of the Indian Association of Pediatric Surgeons                           
Year : 2020  |  Volume : 25  |  Issue : 4  |  Page : 251--253

Giant phyllodes tumor in ectopic breast tissue


Umesh Bahadur Singh1, Jai K Mahajan1, Kim Vaiphei2,  
1 Department of Pediatric Surgery, Postgraduate Institute of Medical Education and Research, Chandigarh, India
2 Department of Histopathology, Postgraduate Institute of Medical Education and Research, Chandigarh, India

Correspondence Address:
Dr. Jai K Mahajan
Department of Pediatric Surgery, Advanced Pediatric Centre, Postgraduate Institute of Medical Education and Research, Chandigarh
India

Abstract

Breast masses are uncommon in children and adolescents. Ectopic breast tissue is further uncommon and may be present in locations such as the face, back, and thigh. A 12-year-old female child presented with a hard, nonmobile lump in the right breast. On exploration by submammary incision, the lump was found to be below the pectoralis major muscle and had no communication with the overlying orthotopic breast tissue. Histopathological examination revealed a well-encapsulated biphasic lesion, with features characteristic of a phyllodes tumor. We report a hitherto unreported case of aberrant breast tissue lying under the pectoralis muscle and containing phyllodes tumor.



How to cite this article:
Singh UB, Mahajan JK, Vaiphei K. Giant phyllodes tumor in ectopic breast tissue.J Indian Assoc Pediatr Surg 2020;25:251-253


How to cite this URL:
Singh UB, Mahajan JK, Vaiphei K. Giant phyllodes tumor in ectopic breast tissue. J Indian Assoc Pediatr Surg [serial online] 2020 [cited 2020 Aug 10 ];25:251-253
Available from: http://www.jiaps.com/text.asp?2020/25/4/251/287652


Full Text



 Introduction



Ectopic breasts have been described as both supernumerary and aberrant breasts. Supernumerary breasts result from a specific process occurring during the embryologic development beginning between the 4th and 5th weeks of gestation. Regression of the mammary ridge occurs at all the places other than the pectoral regions.[1] A supernumerary breast will have a ductal system communicating with the overlying skin, usually located along the “milk line.” This form of ectopic tissue is subject to similar physiological changes of the reproductive cycle as well as diseases and alterations, whether malignant or benign, that affect the orthotopic breasts.[2],[3] The second form of ectopic breast tissue, the aberrant breast, is characterized by an unorganized secretory system without any connection between inside and outside. Axillary location is the most frequently described; however, parasternal, subscapular, and vulvar locations have also been reported.[4],[5] Unlike supernumerary breasts, aberrant breasts have no organized secretory system and do not bear any relationship to their overlying skin.[5] In ectopic breast tissue, malignant transformations have been reported to occur more frequently than the benign diseases.[1],[4],[5]

Breast masses are uncommon in children and adolescents, with a prevalence of 3.2% in teenage girls. Ninety-five percent of the operated masses in pediatric breast are benign fibroadenomas, whereas only 0.02% are malignant.[6] Ectopic location of breast tissue in retropectoral plane and phyllodes tumor occurring in the ectopic breast tissue have not been described earlier.

 Case Report



A 12-year-old female child presented with gradual enlargement of the right breast for the past 2 months. There was no history of breast cancer in the family, and the menarche had not been attained yet. On examination, the breasts were asymmetrically enlarged, and there was no nipple discharge, ulceration, cutaneous edema, or nipple retraction. On palpation, a deep-seated, slightly tender, hard lump with restricted mobility was felt within the soft superficial breast tissue, measuring approximately 10 cm × 9 cm. Ultrasonogram of the right breast and axilla showed an oval, well-circumscribed, homogenously isoechoic mass lesion with smooth margins, measuring 9 cm × 7 cm, occupying all the four quadrants and normal breast tissue being seen superficial to it. Fine-needle aspiration cytology showed staghorn clusters of benign ductal epithelial cells and scattered bipolar nuclei in fibromyxoid background suggestive of fibroadenoma without significant nuclear atypia, necrosis, and mitosis.

On surgery, the mass was found behind the pectoral muscle separately from the orthotopic breast tissue and was excised by submammary incision [Figure 1]a. Histopathological examination revealed a well-encapsulated biphasic lesion comprising both epithelial and stromal components. The stromal component was composed of proliferating spindle cells compressing the epithelial component at places. The stromal component showed a leaf-like overgrowth and perinodal condensation of the stromal cells, whereas the epithelial component had acini-like structures. No atypia or mitosis was seen. The overall features were suggestive of a phyllodes tumor [Figure 1]b.{Figure 1}

 Discussion



Ectopic breast, also referred to as “accessory breast,” has been classified into eight types according to the presence of a nipple, areola, and/or glandular tissue. Copeland and Geschickter proposed a more convenient classification; they referred to the persistent or atrophic glandular tissue with a nipple or areola as supernumerary breast, and the aberrant breast to be mammary tissue alone without a nipple or areolar complex.[7]

Benign or malignant degeneration of ectopic breast tissue has been reported to be highly probable. Phyllodes tumor is a rare lesion of the breast (0.3% of all breast tumors) and has bimodal prevalence between the ages of 30 and 50 years. The tumor generally occurs only once, and if it occurs in a high-risk population, the risk of breast cancer increases significantly even before the age of 35 years. Phyllodes tumor manifests as a painless breast mass, as also seen in this index case, or patients may have a history of sudden enlargement of a previously stable mass, causing thinning of the overlying skin and increased vascularity. These are difficult to distinguish clinically from the giant fibroadenomas. Ultrasonography may not usually distinguish between fibroadenoma and a phyllodes tumor; however, the differentiation can be made by histologic examination, with phyllodes tumors having more cellular stroma, nuclear atypia, and mitotic figures. As many as 25% of the phyllodes tumors are considered malignant. In large tumors, the heterogeneity in cellularity across the spectrum of fibroadenoma and phyllodes tumor can be seen and therefore, excision is indicated. High-grade tumors have increased mitotic rate and show similarity to sarcomas. Despite histologic classification, all phyllodes tumors (benign, intermediate, and malignant) have potential to metastasize and recur locally. Adult 5-year survival rates for benign, intermediate, and malignant phyllodes tumors are 96%, 74%, and 66%, respectively; however, these incidences are unknown in adolescent and pediatric patients. Phyllodes tumors should be treated with complete surgical resection. In adults, a 1-cm surgical margin is recommended. However, adolescent phyllodes tumor seems to be less aggressive, and a smaller surgical margin may be acceptable.

Declaration of patient consent

The authors certify that they have obtained all appropriate patient consent forms. In the form, the patient's guardian has given his consent for his child's images and other clinical information to be reported in the journal. The patient's guardian understands that the child's name and initial will not be published, and due efforts will be made to conceal the child's identity, but anonymity cannot be guaranteed.

Financial support and sponsorship

Nil.

Conflicts of interest

There are no conflicts of interest.

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