Uncommon breast tumors. A report of four cases

Breast cancer is the most common malignancy and the second leading cause of cancer mortality in women, forcing the determination of an early and accurate diagnosis. There are also other uncommon neoplastic lesions. On account that many of them have different prognosis and treatment, it is impor...

Descripción completa

Detalles Bibliográficos
Autores principales: Taddei, E, Ferro, AA, Szlabi, S, Rosetti, D, Cremonezzi, DC
Formato: Artículo revista
Publicado: Universidad Nacional Córdoba. Facultad de Ciencias Médicas. Secretaria de Ciencia y Tecnología 2022
Materias:
Acceso en línea:https://revistas.unc.edu.ar/index.php/med/article/view/39103
Aporte de:
id I10-R327-article-39103
record_format ojs
institution Universidad Nacional de Córdoba
institution_str I-10
repository_str R-327
container_title_str Revista de la Facultad de Ciencias Médicas de Córdoba
format Artículo revista
topic breast
liposarcoma
angiosarcoma
myofibroblastoma
adenomyoepithelioma
MAMA
liposarcoma
angiosarcoma
miofibroblastoma
adenomioepitelioma
spellingShingle breast
liposarcoma
angiosarcoma
myofibroblastoma
adenomyoepithelioma
MAMA
liposarcoma
angiosarcoma
miofibroblastoma
adenomioepitelioma
Taddei, E
Ferro, AA
Szlabi, S
Rosetti, D
Cremonezzi, DC
Uncommon breast tumors. A report of four cases
topic_facet breast
liposarcoma
angiosarcoma
myofibroblastoma
adenomyoepithelioma
MAMA
liposarcoma
angiosarcoma
miofibroblastoma
adenomioepitelioma
author Taddei, E
Ferro, AA
Szlabi, S
Rosetti, D
Cremonezzi, DC
author_facet Taddei, E
Ferro, AA
Szlabi, S
Rosetti, D
Cremonezzi, DC
author_sort Taddei, E
title Uncommon breast tumors. A report of four cases
title_short Uncommon breast tumors. A report of four cases
title_full Uncommon breast tumors. A report of four cases
title_fullStr Uncommon breast tumors. A report of four cases
title_full_unstemmed Uncommon breast tumors. A report of four cases
title_sort uncommon breast tumors. a report of four cases
description Breast cancer is the most common malignancy and the second leading cause of cancer mortality in women, forcing the determination of an early and accurate diagnosis. There are also other uncommon neoplastic lesions. On account that many of them have different prognosis and treatment, it is important to differentiate them. The objective of this work is to interpret the morphology of 4 cases of exceptional presentation, in order to consider them in medical practice. Case 1: 30yo woman, tumor in right upper-outer quadrant. Biopsy: compatible with signet-ring cell carcinoma. In 6mo it grew considerably and a simple mastectomy was performed. We observed a whitish and ulcerated tumor of 24x22x8 cm. Microscopy: mesenchymal neoplasm, marked anisokaryosis, vacuolated cytoplasm, bizarre nuclei, increased mitoses, necrosis, and ulcerated skin. Triple-negative, Ki-67 30%. Diagnosis: Primary pleomorphic liposarcoma. Case 2: 63yo woman with a left painless multinodular mass. Simple mastectomy. Intraoperative biopsy: myxoid spindle cell lesion. Macroscopy: 25 cm tumor, lobulated and pseudoencapsulated. Cut surface is solid, grayish, with mucinous areas and necrohemorrhagic foci. Microscopy: spindle cells, clear cytoplasms, small, hyperchromatic nuclei, inconspicuous nucleoli, nuclear pseudoinclusions, myxoid background, collagenous areas, scarce mitoses. CD34(+), ASMA(+), Ki-67 15%. Diagnosis: Breast myofibroblastoma. Case 3: 82yo woman with a verruciform mass on the skin of the right breast. Macroscopy: 1.4x1x0.9 cm lesion, reddish brown, well-defined borders. At the surgical limit, another elevated lesion is observed, 1.3x9x0.5 cm, whitish, ulcerated. Microscopy: dermis with atypical neoplastic endothelial cells, forming dilated vessels and papillae, Others are spindle-shaped and epithelioid. Diagnosis: High grade angiosarcoma. Case 4: 42yo woman, right painless palpable mass. Quadrantectomy. Macroscopy: 0.6 cm multilobulated, irregular, whitish lesion with central cystification. Microscopy: lobular tubulo-epithelial structures surrounded by basal and interstitial myoepithelial cells with clear, polygonal, and fused cytoplasm. p63(+), Actin(+), Vimentin(+), low Ki-67. Diagnosis: lobulated adenomyoepithelioma Uncommon cases of neoplasms require specific morphological criteria and resolution with immunohistochemical techniques in most cases. Diagnoses must be confirmed with histopathological study and eventually with immunohytochemistry.
publisher Universidad Nacional Córdoba. Facultad de Ciencias Médicas. Secretaria de Ciencia y Tecnología
publishDate 2022
url https://revistas.unc.edu.ar/index.php/med/article/view/39103
work_keys_str_mv AT taddeie uncommonbreasttumorsareportoffourcases
AT ferroaa uncommonbreasttumorsareportoffourcases
AT szlabis uncommonbreasttumorsareportoffourcases
AT rosettid uncommonbreasttumorsareportoffourcases
AT cremonezzidc uncommonbreasttumorsareportoffourcases
AT taddeie tumoresinfrecuentesdelamamacomunicacionde4casos
AT ferroaa tumoresinfrecuentesdelamamacomunicacionde4casos
AT szlabis tumoresinfrecuentesdelamamacomunicacionde4casos
AT rosettid tumoresinfrecuentesdelamamacomunicacionde4casos
AT cremonezzidc tumoresinfrecuentesdelamamacomunicacionde4casos
first_indexed 2024-09-03T21:04:13Z
last_indexed 2024-09-03T21:04:13Z
_version_ 1809210360586043392
spelling I10-R327-article-391032024-04-15T16:14:45Z Uncommon breast tumors. A report of four cases Tumores infrecuentes de la mama. Comunicación de 4 casos Taddei, E Ferro, AA Szlabi, S Rosetti, D Cremonezzi, DC breast liposarcoma angiosarcoma myofibroblastoma adenomyoepithelioma MAMA liposarcoma angiosarcoma miofibroblastoma adenomioepitelioma Breast cancer is the most common malignancy and the second leading cause of cancer mortality in women, forcing the determination of an early and accurate diagnosis. There are also other uncommon neoplastic lesions. On account that many of them have different prognosis and treatment, it is important to differentiate them. The objective of this work is to interpret the morphology of 4 cases of exceptional presentation, in order to consider them in medical practice. Case 1: 30yo woman, tumor in right upper-outer quadrant. Biopsy: compatible with signet-ring cell carcinoma. In 6mo it grew considerably and a simple mastectomy was performed. We observed a whitish and ulcerated tumor of 24x22x8 cm. Microscopy: mesenchymal neoplasm, marked anisokaryosis, vacuolated cytoplasm, bizarre nuclei, increased mitoses, necrosis, and ulcerated skin. Triple-negative, Ki-67 30%. Diagnosis: Primary pleomorphic liposarcoma. Case 2: 63yo woman with a left painless multinodular mass. Simple mastectomy. Intraoperative biopsy: myxoid spindle cell lesion. Macroscopy: 25 cm tumor, lobulated and pseudoencapsulated. Cut surface is solid, grayish, with mucinous areas and necrohemorrhagic foci. Microscopy: spindle cells, clear cytoplasms, small, hyperchromatic nuclei, inconspicuous nucleoli, nuclear pseudoinclusions, myxoid background, collagenous areas, scarce mitoses. CD34(+), ASMA(+), Ki-67 15%. Diagnosis: Breast myofibroblastoma. Case 3: 82yo woman with a verruciform mass on the skin of the right breast. Macroscopy: 1.4x1x0.9 cm lesion, reddish brown, well-defined borders. At the surgical limit, another elevated lesion is observed, 1.3x9x0.5 cm, whitish, ulcerated. Microscopy: dermis with atypical neoplastic endothelial cells, forming dilated vessels and papillae, Others are spindle-shaped and epithelioid. Diagnosis: High grade angiosarcoma. Case 4: 42yo woman, right painless palpable mass. Quadrantectomy. Macroscopy: 0.6 cm multilobulated, irregular, whitish lesion with central cystification. Microscopy: lobular tubulo-epithelial structures surrounded by basal and interstitial myoepithelial cells with clear, polygonal, and fused cytoplasm. p63(+), Actin(+), Vimentin(+), low Ki-67. Diagnosis: lobulated adenomyoepithelioma Uncommon cases of neoplasms require specific morphological criteria and resolution with immunohistochemical techniques in most cases. Diagnoses must be confirmed with histopathological study and eventually with immunohytochemistry. El cáncer de mama es la neoplasia maligna más frecuente y la segunda causa de mortalidad por cáncer en mujeres, obligando a la determinación de un diagnóstico precoz y certero. Existen además otras lesiones neoplásicas infrecuentes. Debido a que muchas de ellas tienen distinto pronóstico y tratamiento, es importante diferenciarlas. El objetivo de este trabajo es interpretar la morfología de 4 casos de presentación excepcional, a fin de considerarlos en la práctica médica. Caso 1: Mujer de 30a, tumor en cuadrante supero-externo derecho. Biopsia: compatible con carcinoma en anillo de sello. En 6m creció considerablemente y se realizó mastectomía simple. Observamos un tumor blanquecino y ulcerado de 24x22x8 cm. Microscopía: neoplasia mesenquimal, marcada anisocariosis, citoplasmas vacuolados, núcleos bizarros, mitosis incrementadas, necrosis y piel ulcerada. Triple negativo, Ki67 30%. Diagnóstico: Liposarcoma pleomórfico primario. Caso 2: Mujer de 63a con masa multinodular indolora izquierda. Mastectomía simple. Biopsia intraoperatoria: lesión fusocelular mixoide. Macroscopía: tumor de 25 cm, lobulado y pseudoencapsulado. Al corte es sólido, grisáceo, áreas mucinosas y focos necrohemorrágicos. Microscopía: células fusiformes, citoplasmas claros, núcleos pequeños, hipercromáticos, nucléolos inconspicuos, pseudoinclusiones nucleares, fondo mixoide, áreas colágenas, mitosis escasas. CD34(+), ASMA(+), Ki-67 15%. Diagnóstico: Miofibroblastoma mamario. Caso 3: Mujer, 82a con masa verruciforme en piel de mama derecha. Macroscopía: lesión de 1,4x1x0,9 cm, pardo rojiza, bordes netos. En límite quirúrgico se observa otra lesión sobreelevada, de 1,3x9x0,5 cm, blanquecina, ulcerada. Microscopía: dermis con células neoplásicas endoteliales atípicas, fusadas y epitelioides, formando vasos dilatados y papilas. Diagnóstico: Angiosarcoma de alto grado. Caso 4: Mujer, 42a, masa palpable indolora derecha. Cuadrantectomía. Macroscopía: lesión multilobulada de 0,6 cm, irregular, blanquecina, quistificación central. Microscopía: estructuras lobulares túbulo-epiteliales rodeadas por células mioepiteliales basales e intersticiales; de citoplasmas claros, poligonales y fusados. P63(+), Actina(+), Vimentina(+), Ki-67 bajo. Diagnóstico: Adenomioepitelioma lobular. Los casos de neoplasias infrecuentes necesitan criterios morfológicos específicos y resolución con técnicas de inmunohistoquímica en la mayoría de los casos. Los diagnósticos deben confirmarse con el estudio histopatológico y eventualmente con inmunohitoquímica. Universidad Nacional Córdoba. Facultad de Ciencias Médicas. Secretaria de Ciencia y Tecnología 2022-10-26 info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion texto https://revistas.unc.edu.ar/index.php/med/article/view/39103 Revista de la Facultad de Ciencias Médicas de Córdoba.; Vol. 79 No. Suplemento JIC XXIII (2022): Suplemento JIC XXIII Revista de la Facultad de Ciencias Médicas de Córdoba; Vol. 79 Núm. Suplemento JIC XXIII (2022): Suplemento JIC XXIII Revista da Faculdade de Ciências Médicas de Córdoba; v. 79 n. Suplemento JIC XXIII (2022): Suplemento JIC XXIII 1853-0605 0014-6722 http://creativecommons.org/licenses/by-nc/4.0