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1.
Br J Radiol ; 97(1157): 1057-1065, 2024 May 07.
Artículo en Inglés | MEDLINE | ID: mdl-38402483

RESUMEN

OBJECTIVE: To explore the value of magnetic resonance imaging (MRI) and clinical features in identifying ovarian thecoma-fibroma (OTF) with cystic degeneration and ovary adenofibroma (OAF). METHODS: A total of 40 patients with OTF (OTF group) and 28 patients with OAF (OAF group) were included in this retrospective study. Univariable and multivariable analyses were performed on clinical features and MRI between the two groups, and the receiver operating characteristic (ROC) curve was plotted to estimate the optimal threshold and predictive performance. RESULTS: The OTF group had smaller cyst degeneration degree (P < .001), fewer black sponge sign (20% vs. 53.6%, P = .004), lower minimum apparent diffusion coefficient value (ADCmin) (0.986 (0.152) vs. 1.255 (0.370), P < .001), higher age (57.4 ± 14.2 vs. 44.1 ± 15.9, P = .001) and more postmenopausal women (72.5% vs. 28.6%, P < .001) than OAF. The area under the curve of MRI, clinical features and MRI combined with clinical features was 0.870, 0.841, and 0.954, respectively, and MRI combined with clinical features was significantly higher than the other two (P < .05). CONCLUSION: The cyst degeneration degree, black sponge sign, ADCmin, age and menopause were independent factors in identifying OTF with cystic degeneration and OAF. The combination of MRI and clinical features has a good effect on the identification of the two. ADVANCES IN KNOWLEDGE: This is the first time to distinguish OTF with cystic degeneration from OAF by combining MRI and clinical features. It shows the diagnostic performance of MRI, clinical features, and combination of the two. This will facilitate the discriminability and awareness of these two diseases among radiologists and gynaecologists.


Asunto(s)
Adenofibroma , Imagen por Resonancia Magnética , Neoplasias Ováricas , Neoplasia Tecoma , Humanos , Femenino , Persona de Mediana Edad , Estudios Retrospectivos , Diagnóstico Diferencial , Neoplasias Ováricas/diagnóstico por imagen , Neoplasias Ováricas/patología , Imagen por Resonancia Magnética/métodos , Neoplasia Tecoma/diagnóstico por imagen , Neoplasia Tecoma/patología , Adulto , Adenofibroma/diagnóstico por imagen , Adenofibroma/patología , Fibroma/diagnóstico por imagen , Anciano , Quistes Ováricos/diagnóstico por imagen
4.
Medicine (Baltimore) ; 102(8): e32965, 2023 Feb 22.
Artículo en Inglés | MEDLINE | ID: mdl-36827035

RESUMEN

RATIONALE: Endometrioid adenofibroma is a benign epithelial neoplasm of the ovary, most of which are often unilateral. The symptoms of endometrioid adenofibroma are often nonspecific and misleading. Therefore, a full understanding of the characteristics, diagnosis, and treatment methods of this disease is of great importance. In this study, we report a 34-year-old woman who was found with an unidentified mass on the right ovary during the physical examination 3 years ago with nosymptoms or signs. PATIENT CONCERNS: A 34-year-old Chinese female was found with an unidentified 6 cm mass on the right ovary for 3 years that presented with no symptoms or signs. DIAGNOSIS: Pelvic ultrasound revealed a 6 cm cystic solid mixed mass on the right ovary. Through histological and immunohistochemical examinations, the tumor mass was finally diagnosed as endometrioid adenofibroma of ovary. INTERVENTIONS: To confirm the diagnosis, the ovarian tumor was laparoscopically resected. OUTCOMES: The patient returned to hospital after 3 months with no recurrence or postoperative complications. LESSONS: Endometrioid adenofibroma is a benign epithelial neoplasm of the ovary. Complete surgical resection is required and rare cases can recur. Postsurgical pathologic and immunohistochemical testing can confirm a diagnosis of endometrioid adenofibroma. It is important to understand of the key points of differential diagnosis of the disease due to the different prognosis and clinical treatment.


Asunto(s)
Adenofibroma , Neoplasias Glandulares y Epiteliales , Neoplasias Ováricas , Femenino , Humanos , Adulto , Neoplasias Ováricas/patología , Neoplasias Glandulares y Epiteliales/diagnóstico , Diagnóstico Diferencial , Adenofibroma/diagnóstico , Adenofibroma/patología , Adenofibroma/cirugía
6.
BMC Med Imaging ; 22(1): 47, 2022 03 17.
Artículo en Inglés | MEDLINE | ID: mdl-35296268

RESUMEN

BACKGROUND: Biliary adenofibroma (BAF) is a rare primary hepatic tumor with the potential risk of malignant transformation. Given the extreme rarity of the disease, the imaging features of BAF are unclear. We presented a case of malignant BAF and conducted a systematic literature review. We highlighted the key imaging features in the diagnosis and aggressiveness assessment of BAF, as well as the role of various imaging modalities in evaluating BAF. CASE PRESENTATION: We reported a 64-year-old woman with a 5-months history of pain in the right upper quadrant abdomen. US of the liver showed a hypoechoic subcapsular nodule. CT scan revealed a subcapsular solid-cystic mass in segment V of the liver. The mass showed a marked enhancement in the arterial phase followed by wash-out in the venous phase. The patient underwent partial resection of liver's right lobe. The mass was diagnosed as BAF with malignant transformation by postoperative pathology. CONCLUSIONS: CT and MRI are helpful in recognizing and characterizing BAF. The imaging features of BAF include a solitary, large solid-cystic mass with a well-defined margin, lobulated shape, and internal septa; subcapsular location; no intrahepatic bile duct communication; the presence of von Meyenberg complexes in background liver. The enhancement patterns may have the potential to assess the aggressiveness of BAF, and that marked enhancement in the arterial phase followed by wash-out in the venous phase is suggestive of malignant BAF.


Asunto(s)
Adenofibroma , Neoplasias Gastrointestinales , Neoplasias Hepáticas , Abdomen , Adenofibroma/diagnóstico por imagen , Adenofibroma/patología , Adenofibroma/cirugía , Femenino , Humanos , Neoplasias Hepáticas/diagnóstico por imagen , Neoplasias Hepáticas/cirugía , Persona de Mediana Edad , Tomografía Computarizada por Rayos X
7.
Int J Gynecol Pathol ; 41(1): 76-81, 2022 Jan 01.
Artículo en Inglés | MEDLINE | ID: mdl-33741765

RESUMEN

Ovarian seromucinous borderline tumors (SMBT) and clear cell tumors are both closely associated with endometriosis and share, in a proportion of cases, a molecular pathway involving ARID1A mutations, but they have been rarely described in association. We report a case series of 4 clear cell tumors (3 carcinomas, 1 borderline adenofibroma) coexisting in the same ovary with SMBT. In all cases, the SMBT was the predominant component and we highlight that adequate sampling of these tumors is important to detect small clear cell carcinomas, thus potentially altering the treatment and prognosis.


Asunto(s)
Adenocarcinoma Mucinoso/diagnóstico , Adenofibroma/diagnóstico , Carcinoma Epitelial de Ovario/diagnóstico , Proteínas de Unión al ADN/metabolismo , Endometriosis/diagnóstico , Neoplasias Ováricas/diagnóstico , Factores de Transcripción/metabolismo , Adenocarcinoma Mucinoso/complicaciones , Adenocarcinoma Mucinoso/patología , Adenofibroma/complicaciones , Adenofibroma/patología , Adulto , Anciano , Carcinoma Epitelial de Ovario/complicaciones , Carcinoma Epitelial de Ovario/patología , Proteínas de Unión al ADN/genética , Endometriosis/complicaciones , Endometriosis/patología , Femenino , Humanos , Persona de Mediana Edad , Mutación , Neoplasias Ováricas/complicaciones , Neoplasias Ováricas/patología , Ovario/patología , Factores de Transcripción/genética
8.
J Nippon Med Sch ; 88(6): 564-568, 2021.
Artículo en Inglés | MEDLINE | ID: mdl-34980742

RESUMEN

Pulmonary adenofibroma is a rare biphasic tumor that contains epithelial and stromal components. We report a case of pulmonary adenofibroma in which the tumor was resected by thoracoscopic surgery and the diagnosis was established by histopathology. A 59-year-old woman with a past medical history of pyelonephritis visited our hospital for evaluation of an abnormal opacity on a plain chest x-ray during a comprehensive medical examination. A follow-up chest x-ray showed enlargement of the lesion, and the patient was referred to our department for further management. Chest computed tomography revealed a well-circumscribed nodule measuring 1.4 cm in diameter in the upper lobe of the left lung. The chest imaging findings suggested a benign tumor, but because of evidence of lesion enlargement and elevated serum carcinoembryonic antigen levels, we performed wide wedge resection of the left upper lobe by video-assisted thoracoscopic surgery, for diagnosis and treatment. The resected specimen was submitted for rapid pathological diagnosis during the operation, and a benign tumor, possibly sclerosing pneumocytoma, was suspected. Therefore, we completed the operation with wide wedge resection. The final histopathological diagnosis was pulmonary adenofibroma. The patient had an uneventful postoperative course, and at this writing, 6 months postoperatively, there has been no evidence of tumor recurrence. We have reported this case of pulmonary adenofibroma because the tumor is rare, has not yet been well-characterized, and has an unclear prognosis. Collection of data from a larger number of patients is necessary.


Asunto(s)
Adenofibroma/cirugía , Neoplasias Pulmonares/cirugía , Cirugía Torácica Asistida por Video/métodos , Adenofibroma/diagnóstico por imagen , Adenofibroma/patología , Femenino , Humanos , Neoplasias Pulmonares/diagnóstico por imagen , Neoplasias Pulmonares/patología , Persona de Mediana Edad , Recurrencia Local de Neoplasia , Hemangioma Esclerosante Pulmonar , Resultado del Tratamiento
9.
J Cutan Pathol ; 48(2): 330-333, 2021 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-32809225

RESUMEN

Dermatofibromas (DF) are common skin lesions composed of a dermal proliferation of fibroblasts and histiocytes. Among the variants of DFs, adenodermatofibroma are characterized by a dense proliferation of fibroblasts and histiocytes admixed with entrapped dilated glandular structures. We report two additional cases of adenodermatofibromas, review the literature, theorize on the histopathogenesis of this variant, and suggest that there are different patterns among adenodermatofibromas, from primarily cystic to primarily glandular.


Asunto(s)
Adenofibroma , Proliferación Celular , Fibroblastos , Histiocitos , Neoplasias Cutáneas , Adenofibroma/metabolismo , Adenofibroma/patología , Adulto , Anciano , Fibroblastos/metabolismo , Fibroblastos/patología , Histiocitos/metabolismo , Histiocitos/patología , Humanos , Masculino , Neoplasias Cutáneas/metabolismo , Neoplasias Cutáneas/patología
10.
Histopathology ; 78(3): 445-452, 2021 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-32810322

RESUMEN

AIMS: To report a series of benign ovarian seromucinous neoplasms, an uncommon and hitherto poorly described category of tumours included in the current 2014 World Health Organisation classification of tumours of the female reproductive organs. METHODS AND RESULTS: We report the clinicopathological features of a series of 22 benign ovarian seromucinous neoplasms (cystadenomas and adenofibromas or admixtures). The neoplasms occurred in patients aged 32-83 years (mean = 62, median = 65.5) and involved the left ovary (n = 14), the right ovary (n = 6) or both ovaries (n = 2). There was a common association with endometrioid elements (endometrioid differentiation within the cystadenoma/adenofibroma and/or endometriosis) and other endometriosis-associated neoplasms. CONCLUSIONS: We speculate that some of these represent benign ovarian endometrioid neoplasms with foci of mucinous and/or serous differentiation, while others represent true mixed neoplasms.


Asunto(s)
Adenofibroma/patología , Cistoadenoma/patología , Neoplasias Ováricas/patología , Adulto , Anciano , Anciano de 80 o más Años , Endometriosis/patología , Femenino , Humanos , Persona de Mediana Edad , Neoplasias/patología , Ovario/patología
11.
BMJ Case Rep ; 13(6)2020 Jun 09.
Artículo en Inglés | MEDLINE | ID: mdl-32522722

RESUMEN

Serous adenofibroma of the fallopian tube is a rare, benign tumour of the female genital tract. They are usually small, asymptomatic and incidentally diagnosed during a surgery for another gynaecological condition. This report presents an atypical case of a 17-year-old girl with a tubal serous adenofibroma that presented with a palpable mass occupying the entire abdomen accompanied by urinary symptoms. She underwent a laparoscopic surgery with drainage of 1800 mL of yellow, citrine liquid from the cyst and left salpingectomy with no complications.


Asunto(s)
Adenofibroma , Neoplasias de las Trompas Uterinas , Paracentesis/métodos , Salpingectomía/métodos , Adenofibroma/patología , Adenofibroma/fisiopatología , Adenofibroma/cirugía , Adolescente , Diagnóstico Diferencial , Neoplasias de las Trompas Uterinas/patología , Neoplasias de las Trompas Uterinas/fisiopatología , Neoplasias de las Trompas Uterinas/cirugía , Trompas Uterinas/patología , Trompas Uterinas/cirugía , Femenino , Humanos , Imagen por Resonancia Magnética/métodos , Cuidados Preoperatorios/métodos , Resultado del Tratamiento , Carga Tumoral , Ultrasonografía/métodos
12.
Virchows Arch ; 477(2): 195-205, 2020 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-32193604

RESUMEN

As one of the most common target organs for hematogenous spread from diverse cancers, biopsy interpretation of lung tumors is complicated by the challenging question of primary versus metastatic and by frequent entrapment of native respiratory glands. Nevertheless, the literature dealing with this issue is surprisingly sparse and no single study has been devoted to this topic. We reviewed 47 surgical lung specimens of non-epithelial neoplasms (38 metastases, mainly from sarcomas and 9 primary lesions) for frequency and pattern of intralesional epithelial entrapment. Respiratory epithelium entrapment was noted in 23/47 (49%) cases (diffuse in 15 and peripheral in 8). Entrapped glands frequently showed prominent regenerative and reactive changes mimicking neoplastic glands. Based on cellularity of the mesenchymal component and the extent, distribution and shape of entrapped respiratory glands, four morphological patterns were recognized: paucicellular sclerosing low-grade neoplasms containing leaflet-like glands indistinguishable from adenofibroma and fibroepithelial hamartomas (n = 11), and biphasic cellular lesions mimicking adenomyoepithelioma (n = 1), biphasic synovial sarcoma (n = 2), and pleuropulmonary blastoma (n = 1). Only a single genuine pulmonary adenofibroma was identified. This study highlights frequent respiratory epithelium entrapment in diverse non-epithelial lung tumors, both primary and metastatic. Recognition of this finding and use of adjunct IHC combined with clinical history should help to avoid misinterpretation as primary pulmonary biphasic neoplasm or as harmless adenofibroma. The vast majority of morphologically defined lung adenofibromas represent adenofibroma-like variants of histogenetically diverse entities so that a diagnosis of adenofibroma should be rendered only very restrictively and then as a diagnosis by exclusion.


Asunto(s)
Adenofibroma/patología , Diagnóstico Diferencial , Neoplasias Pulmonares/patología , Mucosa Respiratoria/patología , Adenofibroma/diagnóstico , Adolescente , Adulto , Anciano , Biomarcadores de Tumor/análisis , Femenino , Humanos , Neoplasias Pulmonares/diagnóstico , Masculino , Persona de Mediana Edad , Metástasis de la Neoplasia , Adulto Joven
13.
Am J Surg Pathol ; 44(7): 917-921, 2020 07.
Artículo en Inglés | MEDLINE | ID: mdl-32091433

RESUMEN

Thirteen cases of primary pulmonary adenofibromas are presented. The patients are 8 women and 5 men between the ages of 41 and 73 years (average: 57 y). The patients presented with nonspecific symptomatology or their tumor was identified during routine chest films. A wedge resection was performed in all cases with lymph node sampling. Grossly, the tumors varied in size from 1 to 2.5 cm in greatest dimension. The entire tumor was histologically evaluated in all cases. All the tumors shared similar histologic features namely leaf-like/phyllodes-like growth patterns with varying areas of sclerosis, focal inflammation, and entrapped epithelium. A wide panel of immunohistochemical studies was performed including epithelial, neural, muscle, and vascular markers, all of which showed negative staining. The tumors were positive only for vimentin in the stroma and keratin in the entrapped epithelium. Further evaluation in 6 cases using in situ hybridization for the solitary fibrous tumor was performed and was negative. Clinical follow-up in all the patients showed no evidence of recurrence or metastatic disease, during a period of 12 to 36 months. The current cases highlight the unusual occurrence of pulmonary adenofibromas and the importance of separating these tumors from other tumors that may have the potential to recur or metastasize. The use of proper immunohistochemical stains/molecular analysis aids in the proper classification of these tumors.


Asunto(s)
Adenofibroma/diagnóstico , Adenofibroma/patología , Neoplasias Pulmonares/diagnóstico , Neoplasias Pulmonares/patología , Adenofibroma/metabolismo , Adenofibroma/cirugía , Adulto , Anciano , Biomarcadores de Tumor/metabolismo , Femenino , Estudios de Seguimiento , Humanos , Inmunohistoquímica , Neoplasias Pulmonares/metabolismo , Neoplasias Pulmonares/cirugía , Masculino , Persona de Mediana Edad , Neumonectomía , Pronóstico
14.
Korean J Gastroenterol ; 74(6): 356-361, 2019 Dec 25.
Artículo en Inglés | MEDLINE | ID: mdl-31870142

RESUMEN

Biliary adenofibroma is a rare tumor with a bile duct origin characterized by a complex tubulocystic non-mucin secreting biliary epithelium with abundant fibrous stroma. The MRI features of biliary adenofibroma are not well established. The authors encountered two patients with biliary adenofibroma and reviewed the literature focusing on the MRI findings. A well-circumscribed multicystic tumor with septal enhancement and no intrahepatic bile duct communication may be the characteristic MRI findings of biliary adenofibroma.


Asunto(s)
Adenofibroma/diagnóstico , Neoplasias de los Conductos Biliares/diagnóstico , Imagen por Resonancia Magnética , Adenofibroma/complicaciones , Adenofibroma/diagnóstico por imagen , Adenofibroma/patología , Adulto , Neoplasias de los Conductos Biliares/complicaciones , Neoplasias de los Conductos Biliares/diagnóstico por imagen , Neoplasias de los Conductos Biliares/patología , Hepatitis B Crónica/complicaciones , Hepatitis B Crónica/diagnóstico , Humanos , Masculino , Persona de Mediana Edad , Tomografía Computarizada por Rayos X
15.
Mol Cancer Res ; 17(10): 2015-2028, 2019 10.
Artículo en Inglés | MEDLINE | ID: mdl-31308149

RESUMEN

Semaphorins are a large family of evolutionarily conserved morphogenetic molecules that are associated with repelling axonal guidance. Intriguingly, recent researches indicate that semaphorins are involved in cancer progression. Semaphorin 4C (SEMA4C) has long been considered a neuronal migration gene, but we detected that it is also highly expressed in many malignant human cancers. During an investigation of subcutaneous tumor models, we found that SEMA4C expression promoted tumor growth and progression. We discovered that SEMA4C was involved in maintaining tumor cell self-renewal, likely by regulating the p53 pathway. Inhibiting the expression of endogenous SEMA4C in tumor cells impaired growth and induced senescence and cell-cycle arrest in the G2-phase. In addition, we found that SEMA4C induced the production of angiogenin and colony-stimulating factor-1 (CSF-1) in tumor cells by activating the NF-κB pathway in a plexinB2-dependent manner. In conclusion, SEMA4C expression in breast cancer cells promotes cancer cell proliferation, macrophage recruitment, and angiogenesis. Thus, inhibition of SEMA4C activity may be a novel therapeutic strategy for human breast cancer. IMPLICATIONS: In breast cancer, therapeutic targeting of the SEMA4C pathway may prevent tumor growth, angiogenesis, metastasis, and progression.


Asunto(s)
Neoplasias de la Mama/irrigación sanguínea , Neoplasias de la Mama/metabolismo , Macrófagos/metabolismo , Macrófagos/patología , Semaforinas/metabolismo , Células A549 , Adenofibroma/irrigación sanguínea , Adenofibroma/genética , Adenofibroma/metabolismo , Adenofibroma/patología , Animales , Neoplasias de la Mama/genética , Neoplasias de la Mama/patología , Línea Celular Tumoral , Femenino , Células HT29 , Células HeLa , Xenoinjertos , Células Endoteliales de la Vena Umbilical Humana , Humanos , Células MCF-7 , Ratones , Ratones Endogámicos BALB C , Ratones Desnudos , Persona de Mediana Edad , Neovascularización Patológica/metabolismo , Neovascularización Patológica/patología , Proteínas del Tejido Nervioso/metabolismo , Semaforinas/biosíntesis , Semaforinas/genética , Transducción de Señal , Proteína p53 Supresora de Tumor/metabolismo
16.
Radiographics ; 39(4): 982-997, 2019.
Artículo en Inglés | MEDLINE | ID: mdl-31283462

RESUMEN

Mucinous neoplasms of the ovary account for 10%-15% of ovarian neoplasms. They may be benign, borderline, or malignant. The large majority are benign or borderline, accounting for 80% and 16%-17%, respectively. Mucinous neoplasms of the ovary most commonly affect women in their 20s to 40s. The clinical manifestation is nonspecific, but most mucinous ovarian neoplasms manifest as large unilateral pelvic masses. At gross pathologic analysis, mucinous ovarian neoplasms appear as large multiloculated cystic masses. The contents of the cyst loculi vary on the basis of differences in internal mucin content. At histologic analysis, mucinous ovarian neoplasms are composed of multiple cysts lined by mucinous epithelium, often resembling gastrointestinal-type epithelium. Imaging evaluation most commonly includes US and/or MRI. The imaging findings parallel the gross pathologic features and include a large, unilateral, multiloculated cystic mass. The cyst loculi vary in echogenicity, attenuation, and signal intensity depending on the mucin content. Mucinous neoplasms of the ovary are staged surgically using the FIGO (International Federation of Gynecology and Obstetrics) staging system. Primary treatment is surgical, with adjuvant chemotherapy considered in the uncommon case of mucinous carcinoma with extraovarian disease. Since most mucinous ovarian neoplasms are benign or borderline, the overall prognosis is excellent.


Asunto(s)
Adenocarcinoma Mucinoso/diagnóstico por imagen , Cistoadenoma Mucinoso/diagnóstico por imagen , Neoplasias Ováricas/diagnóstico por imagen , Tomografía Computarizada por Rayos X/métodos , Ultrasonografía/métodos , Adenocarcinoma Mucinoso/epidemiología , Adenocarcinoma Mucinoso/patología , Adenofibroma/diagnóstico por imagen , Adenofibroma/patología , Adulto , Anciano , Neoplasias del Apéndice/diagnóstico por imagen , Tumor de Brenner/diagnóstico por imagen , Tumor de Brenner/patología , Cistoadenoma Mucinoso/epidemiología , Cistoadenoma Mucinoso/patología , Diagnóstico Diferencial , Epitelio/patología , Femenino , Humanos , Imagen por Resonancia Magnética , Persona de Mediana Edad , Estadificación de Neoplasias , Quistes Ováricos/diagnóstico por imagen , Quistes Ováricos/patología , Neoplasias Ováricas/epidemiología , Neoplasias Ováricas/patología , Tomografía Computarizada por Tomografía de Emisión de Positrones , Carga Tumoral , Adulto Joven
17.
J Vet Med Sci ; 81(3): 486-490, 2019 Mar 30.
Artículo en Inglés | MEDLINE | ID: mdl-30726785

RESUMEN

A solitary firm nodule was found in the lung of a sika deer (Cervus nippon yesoensis). Histologically, it was a biphasic lesion composed of epithelial and stromal cell elements and exhibited a leaf-like growth pattern. The epithelial cells were immunohistochemically positive for pancytokeratin, cytokeratin 7, napsin A, and thyroid transcription factor-1, and the stromal cells were positive for vimentin and partially positive for desmin and α-smooth muscle actin. These observations were consistent with pulmonary adenofibroma, which is an extremely rare lesion in humans. To the best of our knowledge, this is the first reported case of pulmonary adenofibroma in an animal.


Asunto(s)
Adenofibroma/veterinaria , Ciervos , Neoplasias Pulmonares/veterinaria , Adenofibroma/patología , Animales , Femenino , Técnicas para Inmunoenzimas/veterinaria , Neoplasias Pulmonares/patología
18.
Int J Surg Pathol ; 27(3): 322-327, 2019 May.
Artículo en Inglés | MEDLINE | ID: mdl-30360665

RESUMEN

Pulmonary adenofibroma (PAF) is a rare neoplasm that may be related to solitary fibrous tumor (SFT). A subset of PAFs harbor the NAB2-STAT6 fusion that is typical of SFT, but a significant proportion do not. Their distinction is clinically important as SFTs can potentially have an aggressive clinical course, while there has been no report of a PAF behaving in a malignant fashion. We report a case of a 60-year-old male who developed a SFT and PAF in the same lung. The SFT harbored a NAB2-STAT6 fusion, while the PAF did not have any identifiable fusion. This case represents the first instance of a single patient with both of these tumors occurring simultaneously in the same lung.


Asunto(s)
Adenofibroma/patología , Neoplasias Pulmonares/patología , Neoplasias Primarias Múltiples/patología , Tumores Fibrosos Solitarios/patología , Adenofibroma/diagnóstico por imagen , Adenofibroma/genética , Adenofibroma/cirugía , Biomarcadores de Tumor/genética , Humanos , Pulmón/diagnóstico por imagen , Pulmón/patología , Pulmón/cirugía , Neoplasias Pulmonares/diagnóstico por imagen , Neoplasias Pulmonares/genética , Neoplasias Pulmonares/cirugía , Masculino , Persona de Mediana Edad , Neoplasias Primarias Múltiples/diagnóstico por imagen , Neoplasias Primarias Múltiples/genética , Neoplasias Primarias Múltiples/cirugía , Proteínas de Fusión Oncogénica/genética , Neumonectomía , Proteínas Represoras/genética , Factor de Transcripción STAT6/genética , Tumores Fibrosos Solitarios/diagnóstico por imagen , Tumores Fibrosos Solitarios/genética , Tumores Fibrosos Solitarios/cirugía , Tomografía Computarizada por Rayos X
19.
Clin Biochem ; 60: 24-32, 2018 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-30063890

RESUMEN

OBJECTIVE: MicroRNA-331 (miR-331) has shown regulatory activity against several genes whose expression has been claimed to be deregulated in breast tumors, including that of epidermal growth factor receptor 2 (HER2). Herein, the clinical value of miR-331 expression was investigated by analyzing its levels in breast benign and malignant tumors. METHODS: The expression levels of miR-331 were quantified via real-time PCR in 130 malignant and 66 benign breast tissue specimens collected after surgical resection of primary tumors. The generated data were analyzed by applying several statistical tests in order to examine the relationship of miR-331 expression with various established clinicopathological features and survival data of patients. RESULTS: Our data showed that miR-331 was overexpressed in malignant breast tumors compared to their benign counterparts both overall (P = 0.026) and individually when the subgroups of fibroadenoma and invasive ductal carcinoma were analyzed with each other (P = 0.001). ROC curve analysis confirmed the diagnostic value of these variations, providing an AUC value equal to 0.597 (P = 0.026) and 0.663 (P = 0.001), respectively. Furthermore, miR-331 levels were elevated (P = 0.026) in ductal cancerous specimens compared to the lobular ones but failed to correlate with other clinicopathological features or survival data of the breast cancer patients. CONCLUSIONS: Our results provide evidence that miR-331 levels might provide valuable information regarding the differential diagnosis of benign and malignant breast tumors but present no prognostic value for breast cancer.


Asunto(s)
Adenofibroma/genética , Biomarcadores de Tumor/metabolismo , Neoplasias de la Mama/genética , MicroARNs/genética , Adenofibroma/diagnóstico , Adenofibroma/patología , Neoplasias de la Mama/diagnóstico , Neoplasias de la Mama/patología , Carcinoma Ductal de Mama/diagnóstico , Carcinoma Ductal de Mama/genética , Carcinoma Ductal de Mama/patología , Carcinoma Lobular/diagnóstico , Carcinoma Lobular/genética , Carcinoma Lobular/patología , Diagnóstico Diferencial , Femenino , Humanos , Pronóstico , Reacción en Cadena en Tiempo Real de la Polimerasa
20.
Pan Afr Med J ; 29: 140, 2018.
Artículo en Francés | MEDLINE | ID: mdl-30050604

RESUMEN

The Bi-RADS (Breast Imaging Reporting and Data System) classification developed by the ACR (American College of Radiology) is the classification system for radiological images recommended for breast cancer screening. The ACR 4 microcalcification is an indeterminate or suspected abnormality with 2-95% probability of malignancy, according to studies. This disparity pushed us to conduct this retrospective study of 181 patients in the Department of Obstetrics and Gynecology I at the Hassan II University Hospital, Fez, over a period of 5 years. This study aimed to report the histological results of breast lesions radiologically classified as ACR4 in order to assess their radio-histological correlation and to improve therapeutic approach. All patients underwent breast imaging examinations and then anatomopathologic examination was performed using different techniques. There was a clear predominance of benign lesions with a rate of 62% versus 29% of malignant lesions and only 9% were intermediate lesions. Adenofibroma was the most common histological finding (30% of cases), invasive ductal carcinoma was the most frequent malignant lesion (17% of cases). We performed a literature review which showed that our results were in line with findings of other studies, with a positive predictive value of 29%. Nevertheless, ACR classification divided into subcategories 4a, b and c should be used due to the significant number of unnecessary surgical interventions.


Asunto(s)
Enfermedades de la Mama/diagnóstico por imagen , Neoplasias de la Mama/diagnóstico por imagen , Calcinosis/diagnóstico por imagen , Adenofibroma/diagnóstico por imagen , Adenofibroma/epidemiología , Adenofibroma/patología , Adolescente , Adulto , Anciano , Enfermedades de la Mama/epidemiología , Enfermedades de la Mama/patología , Neoplasias de la Mama/epidemiología , Neoplasias de la Mama/patología , Calcinosis/epidemiología , Calcinosis/patología , Carcinoma Intraductal no Infiltrante/diagnóstico por imagen , Carcinoma Intraductal no Infiltrante/epidemiología , Carcinoma Intraductal no Infiltrante/patología , Femenino , Hospitales Universitarios , Humanos , Tamizaje Masivo/métodos , Persona de Mediana Edad , Marruecos/epidemiología , Valor Predictivo de las Pruebas , Estudios Retrospectivos , Adulto Joven
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