TUMOUR – A CASE REPORT Presentor: DR.B.SRIDHAR Post Graduate Department Of General Surgery Government Stanley Medical College & Hospital
Guide: Prof DR.T.SIVAKUMAR MS
Dr.G.CHANDRASEKAR MS Dr.JIM JEBAKUMAR MS INTRODUCTION • Fibroadenoma is considered “giant” when they attain the size more than 5 cm and/or weigh more than 500 grams. Giant fibroadenoma is a rare variant which comprising 4% of all fibroadenomas of which juvenile fibroadenoma constitutes only 0.5%.
• Giant fibroadenomas are extremely rare in pre-
pubertal girls. Through this case report we want to highlight the clinical approach and management of giant fibroadenoma in pre-pubertal girls. CASE REPORT • A 12 years old girl presented with rapidly enlarging right breast for 1 year duration without any history of pain, trauma, fever, anorexia and weight loss. She has not attained her menarche and there was no significant family history. On clinical examination 20 cm × 15 cm well-circumscribed, firm, non- tender and mobile lump was palpable in right breast with left breast being normal. The lump was not fixed to skin or underlying muscle. The overlying skin was tense and shiny with prominent superficial veins. There was no discharge from the nipple, and axillary lymph- adenopathy was absent. CASE REPORT Routine hematological and biochemical examinations were within normal limits. Chest X-ray was normal • Ultrasonography shows large multiple heteroechoic lesion replacing entire breast. Histopathology examination through a Fine needle aspiration biopsy shows impression of fibroadeoma; however, we were unable to exclude a diagnosis of phyllodes tumor and hence surgical excision was required for full analysis. • Surgical excision of left breast lump with preservation of normal breast tissue, skin and nipple-areola complex was carried out. The resected specimen weighed 900 grams with size of 18x12x8 cms .Cut section showed lobulations with slit like spaces, some areas shows cut cabbage appearance. • Section study shows encapsulated neoplasm with hyperplasia of both epithelial and stromal components. The glands were lined by bilayered epithelium with pericanalicular pattern of fibroadenoma and absence of cytological atypia. The final histopathological diagnosis of Giant Juvenile Fibroadenoma of breast was given CASE REPORT
Surgical excision with
breast conservation resulted in very good cosmesis and patient satisfaction. A submammary incision is preferred to provide good cosmesis. She is in regular follow-up after 6 months of surgery and doing well. DISCUSSION • Fibroadenoma is extremely rare in very young children, with the earliest known published case in a 13-month-old girl. Excessive estrogen stimulation and / or receptor sensitivity or reduced levels of estrogen antagonist during puberty have been implicated in pathogenesis. • Important differential diagnosis to be considered are Virginal hypertrophy, phylloides tumour, premature thelarche,lipoma, hamartoma, breast abscess, macrocyst, adenocarcinoma, Pseudo angiomatous stromal hyperplasia,fibrosarcoma and lymphangioma. • Histologically, juvenile fibroadenomas appear more cellular with fewer lobular components than simple fibroadenomas. In contrast to phyllodes tumours, juvenile fibroadenoma often shows hyperplasia of ductal epithelium with lack of leaf-like structure and stromal cell atypia. CONCLUSION Juvenile breast lesions are rare. Multiple factors must be taken into consideration in terms of clinical, physiological, and psychological care and maturation of the adolescent. Counselling of the patient and the parents are key to the management of this pathology along with avoidance of missing any rare malignant pathology.
A surgical approach requires thorough and detailed
planning to ensure a fine balance between adequate resection and the best cosmetic outcome for a developing breast.