A case of breast cancer associated with juvenile papillomatosis of the male breast

Munítiz, Vicente; Illana, Julián; Sola, Joaquı́n; Piñero, Antonio; Zambudio, A. Ríos; Parrilla, Pascual

doi:10.1053/ejso.2000.0988

Cited by 12 publications

(5 citation statements)

References 8 publications

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“…Only 1 case of carcinoma associated with JPB in a 33-year-old man has been reported previously. 28 In this case, JPB was concurrent with invasive and in situ (micropapillary) carcinoma. Per accompanying illustration, the invasive carcinoma appears to be relatively well differentiated; nevertheless, this relatively young patient died of disease 3 years after initial diagnosis, despite aggressive management with mastectomy, chemotherapy, and radiotherapy.…”

Section: Discussionmentioning

confidence: 71%

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Juvenile Papillomatosis (Swiss-Cheese Disease) of Breast in an Adult Male With Sequential Diagnoses of Ipsilateral Intraductal, Invasive, and Widely Metastatic Carcinoma: A Case Report and Review of the Disease in Males

et al. 2017

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Juvenile papillomatosis of the breast (JPB, also known as Swiss cheese disease) is a rare ailment that typically afflicts young females, and presents as a mass-forming lesion. The lesional mass usually comprises multiple cysts and duct stasis, amid a variety of proliferative and nonproliferative epithelial changes. The proliferative changes include papillary hyperplasia, florid hyperplasia, and papillary apocrine hyperplasia. Concurrent carcinoma (either in situ or invasive) is present in approximately 10% of cases at presentation, and subsequent carcinoma (either in situ or invasive) is diagnosed in about 10% of patients. About 20% of patients have a strong family history of breast carcinoma. A total of 10 cases of JPB have been previously reported in males, both children and adults, only one of which, in a 33-year-old, was associated with invasive carcinoma. Here, another case of JPB in a 45-year-old male-one with subsequent sequential diagnoses of ipsilateral intraductal carcinoma, invasive carcinoma, and widely metastatic carcinoma over the course of 15 years-is reported.

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Section: Discussionmentioning

confidence: 71%

“…To date, 10 cases of JPB have been reported in males 14,15,17,23 -28 (Table 1). Five of these patients were of prepubertal age at diagnosis—a phase of life during which breast diseases are extremely uncommon (particularly in males).…”

Section: Discussionmentioning

confidence: 99%

Juvenile Papillomatosis (Swiss-Cheese Disease) of Breast in an Adult Male With Sequential Diagnoses of Ipsilateral Intraductal, Invasive, and Widely Metastatic Carcinoma: A Case Report and Review of the Disease in Males

et al. 2017

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“…The natural history of JP in males is less clear and, to date, only seven cases (two infants) have been reported in the literature (Table I) 7–12. The mean follow‐up after excision of JP in these cases was 16 months (follow‐up was not available in one case 9).…”

Section: Discussionmentioning

confidence: 99%

“…The mean follow‐up after excision of JP in these cases was 16 months (follow‐up was not available in one case 9). One of these patients died of breast carcinoma 10. He was a 33‐year‐old male with a 2‐month history of a nodule in the left breast.…”

Section: Discussionmentioning

confidence: 99%

Juvenile papillomatosis of the breast in a male infant with Noonan Syndrome, café au lait spots, and family history of breast carcinoma

Pacilli

Sebire

Thambapillai

et al. 2005

Pediatric Blood & Cancer

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Juvenile papillomatosis (JP) of the breast is a rare condition, usually affecting women under 30 years of age. Although this is considered a benign lesion, follow-up is recommended for the patient and family since there is an association with a family history of breast carcinoma and increased risk of development of breast carcinoma. We report an infant with JP, Noonan syndrome (NS), café au lait spots, and family history of breast carcinoma. Seven previously reported cases of JP in males exist, two occurring in infants. The association between JP and NS has not been previously reported.

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“…JP is a benign lesion that typically occurs in young women, including some with a family history of breast cancer 3. In males, JP is exceedingly rare, having been reported only on eight occasions 1,4–8. Of these, three occurred prior to 2 years of age and the remainder occurred between ages 11 and 33 years.…”

mentioning

confidence: 99%

Juvenile papillomatosis of the breast associated with neurofibromatosis 1

Tan

Amor

Chow

2006

Pediatric Blood & Cancer

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A case of breast cancer associated with juvenile papillomatosis of the male breast

Cited by 12 publications

References 8 publications

Juvenile Papillomatosis (Swiss-Cheese Disease) of Breast in an Adult Male With Sequential Diagnoses of Ipsilateral Intraductal, Invasive, and Widely Metastatic Carcinoma: A Case Report and Review of the Disease in Males

Juvenile Papillomatosis (Swiss-Cheese Disease) of Breast in an Adult Male With Sequential Diagnoses of Ipsilateral Intraductal, Invasive, and Widely Metastatic Carcinoma: A Case Report and Review of the Disease in Males

Juvenile papillomatosis of the breast in a male infant with Noonan Syndrome, café au lait spots, and family history of breast carcinoma

Juvenile papillomatosis of the breast associated with neurofibromatosis 1

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