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1.
Zhonghua Bing Li Xue Za Zhi ; 52(9): 902-906, 2023 Sep 08.
Artigo em Chinês | MEDLINE | ID: mdl-37670618

RESUMO

Objective: To investigate the histopathological and immunohistochemical characteristics of benign apocrine cystic papillary hyperplasia of the breast with loss of myoepithelial cell layer. Methods: The clinical data, histopathological features and immunohistochemical profile of patients with benign apocrine cystic papillary hyperplasia of breast with loss of myoepithelial cell layer from January 2016 to December 2021 were examined, in which six patients were identified. Results: All six patients were female, aged 36-61 years (median 46 years), who presented with a breast mass; three cases were from the left breast and three cases were from the right breast. Microscopic examination of all cases showed breast hyperplasia with apocrine cysts, accompanied by different degrees of micropapillary and papillary hyperplasia of apocrine cells. One case was associated with lobular carcinoma in situ, and one case was associated with apocrine ductal carcinoma in situ with intraductal dissemination in adenosis. Immunohistochemical staining of CK5/6, p63, SMA, SMMHC, Calponin and CD10 showed complete absence of myoepithelial cell layer surrounding ducts in apocrine cystic papillary hyperplasia. Conclusions: The myoepithelial cells of apocrine cystic papillary hyperplasia of the breast may undergo abnormal changes and may even be completely lost. The diagnosis should be comprehensively considered along with cytomorphological and histological features to avoid overdiagnosis.


Assuntos
Neoplasias da Mama , Células Epiteliais , Glândulas Mamárias Humanas , Papiloma , Feminino , Humanos , Células Epiteliais/patologia , Hiperplasia/patologia , Papiloma/complicações , Papiloma/patologia , Adulto , Pessoa de Meia-Idade , Glândulas Mamárias Humanas/patologia , Neoplasias da Mama/patologia , Carcinoma Lobular/complicações , Carcinoma Ductal/complicações
3.
Zhonghua Yi Xue Za Zhi ; 101(47): 3885-3889, 2021 Dec 21.
Artigo em Chinês | MEDLINE | ID: mdl-34905889

RESUMO

Objective: To evaluate the imaging features of otosclerosis based on10 µm otology CT. Methods: Data of 27 patients with otosclerosis (51 sides) in Beijing Friendship Hospital, Capital Medical University from October 2020 to July 2021 were retrospectively collected, including 9 males and 18 females age ffrom 22 to 70 (42±12) years. All patients underwent 10 µm otology CT examination and surgical treatment. The types, amounts and involved sites of otosclerosis were analyzed and the sensitivity of 10 µm otology CT in diagnosing otosclerosis were evaluated. Results: Fenestral type accounted for 49.0% (25/51 sides), and diffuse type accounted for 51.0% (26/51 sides),and he retrofenestral type without fenestral lesion was not seen. Single lesions accounted for 45.1% (23/51 sides) and multiple lesions accounted for 54.9% (28/51 sides). The incidence of involvement of the fissula ante fenestram and annular ligaments were both 100%. The incidence of involvement of stapes footplate, vestibule, cochlea, round window, inner auditory canal wall, facial nerve canal, stapes muscle and semicircular canal was 60.8% (31 sides), 33.3% (17/51 sides), 21.6% (11/51 sides), 17.6% (9/51 sides), 13.7% (7/51 sides), 9.8% (5/51 sides), 7.8% (4/51 sides) and 5.9% (3/51 sides), respectively. The sensitivity of 10 µm otology CT in diagnosis of otosclerosis was 100%. Conclusion: 10 µm otology CT can fully display the imaging features of otosclerosis, and has the potential to be an effective routine method for otosclerosis.


Assuntos
Otolaringologia , Otosclerose , Cirurgia do Estribo , Adulto , Idoso , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Otosclerose/diagnóstico por imagem , Otosclerose/cirurgia , Estudos Retrospectivos , Tomografia Computadorizada por Raios X , Adulto Jovem
5.
Zhonghua Bing Li Xue Za Zhi ; 48(3): 231-236, 2019 Mar 08.
Artigo em Chinês | MEDLINE | ID: mdl-30831651

RESUMO

Objective: To investigate the clinicopathologic features and possible causes of granulomatous lobular mastitis(GLM). Methods: Three hundred cases of GLM were collected from surgical specimens diagnosed at Longhua Hospital, Shanghai University of Traditional Chinese Medicine from January 2015 to November 2017. Morphologic features were reviewed using HE staining. A total of 116 cases were investigated by Gram staining. The expression of CD3, CD20, CD68, IgG, IgG4, CD38 and CD138 was detected by immunohistochemical staining. Results: The age of the patients was 23 to 47 years and the median age was 32 years. All patients were female, 96.7% (290/300) had a history of lactation.There were 143 cases of left breasts, 138 cases of right breast and 19 cases of bilateral breasts. Serum prolactin increased in 39.7%(119/300) patients. Within 15.7%(47/300) of patients were associated with nodular erythema or joint swelling and pain of the lower extremities. Pathological observation showed that lobular-centric suppurative granulomatous inflammation, accompanied by dilatation of intralobular and interlobular ducts. There were 16 cases accompanied with duct ectasia. Immunohistochemistry showed CD3-positive lymphocytes were more than CD20-positive lymphocytes in the peripheral aggregation zone of neutrophils within granulomatous lesions. Gram positive bacteria were found in the lipid vacuoles of the 51.7%(60/116) patients. Conclusions: GLM has distinctive histologic features. It may be related to corynebacterium infection, or accompanied by the increase of serum prolactin and erythrocyte sedimentation rate. The age, location and history of the disease are importance in the diagnosis and differential diagnosis.


Assuntos
Mama/patologia , Mastite Granulomatosa/patologia , Adulto , Mama/microbiologia , Aleitamento Materno , China , Feminino , Mastite Granulomatosa/sangue , Mastite Granulomatosa/diagnóstico , Mastite Granulomatosa/microbiologia , Humanos , Pessoa de Meia-Idade , Adulto Jovem
6.
Zhonghua Yi Xue Za Zhi ; 99(6): 447-452, 2019 Feb 12.
Artigo em Chinês | MEDLINE | ID: mdl-30786340

RESUMO

Objective: To evaluate the changes of rat renal function and cardiac function after transabdominal subtotal nephrectomy (STNx) and provide an ideal animal model for the study of chronic kidney disease (CKD) and cardiorenal syndrome (CRS). Methods: The SD rats (male, 5-6 weeks) were randomly divided into Sham group (n=10) and STNx group (n=10). The rats from Sham group underwent sham surgery, and the right nephrectomy plus the 2/3 left kidney artery ligation through abdominal incision were performed in the rats from STNx group. Twelve weeks after operation, the rat serum creatinine and renal pathology were examined, the size and fibrosis of cardiac cells were also observed, after the changes of cardiac function being detected by echocardiography. Results: Twelve weeks after the operation, STNx group rats were generally in poor condition, with a emaciated body, absorption of the renal infarct tissue, uneven surface, and residual renal tissue compensatory hypertrophy. The serum creatinine in Sham group and STNx group was (22.10±1.64) µmol/L and (52.80±3.34) µmol/L, respectively, and there was a statistically significant difference between the two groups (P<0.001). Compared with Sham group, the echocardiography results demonstrated that the thickness of left ventricular wall of rats from STNx group increased, the left ventricular volume decreased, and the diastolic and systolic function of left ventricular descended. The HE staining showed that the glomerulus, tubules and interstitial renal morphology were normal in Sham group, and glomerular sclerosis was observed in STNx group. And the Masson staining declared that the renal fibrous tissue distribution was normal in Sham group, and severe renal interstitial fibrosis was observed in STNx group. The wheat germ agglutinin (WGA) staining of myocardial tissue showed that myocardial cells in STNx group were larger than those in Sham group (1.293±0.060 vs 1.000±0.059, P<0.001). Moreover, the HE staining showed that there was partial myocardial tissue necrosis and fibrosis in STNx group, and severe myocardial fibrosis was observed in STNx group by Masson staining. Conclusion: Similar pathophysiological changes in human CKD were observed in the rats CKD model by transabdominal STNx, and the cardiac effects of this model make it an ideal choice to study CRS.


Assuntos
Síndrome Cardiorrenal , Animais , Rim , Masculino , Miocárdio , Nefrectomia , Ratos , Ratos Sprague-Dawley
9.
Zhonghua Bing Li Xue Za Zhi ; 20(3): 201-4, 1991 Sep.
Artigo em Chinês | MEDLINE | ID: mdl-1664303

RESUMO

Forty-one astrocytomas of different grades were studied by means of image analysis technique for measuring DNA content in situ, and in 28 tumors the numbers of nucleolar organiser region (NORs) associated proteins were also determined, and 12 cases of astrocytoma in frontal lobes were followed up. The results showed that the distribution of DNA content in grade I astrocytoma was 2C-4C, the peak values of grade I astrocytoma was 2C; while for grade II, 3C-4C and hypertetraploid. DNA contents of grade III and IV astrocytomas were much higher, their histograms were dispersed with many peaks, the peak values were aneuploid and heteroploid. The data confirm that heteroploid and aneuploid are the marks of malignancy. The grade II astrocytoma which possesses these features has a tendency to higher malignancy. Twenty-eight astrocytomas were stained by Argyrophil (Ag-NOR) for NOR associated proteins. The largest numbers of Ag-NORs were seen in grades III and IV astrocytoma (mean 11.71), and their Ag-NORs were irregular. Grade I astrocytoma possessed the fewest Ag-NORs (mean 6.5) which were small and uniform. The results suggest that the number of Ag-NORs is associated with the differentiation. The prognosis is significantly correlated with the numbers of Ag-NORs and the contents of DNA in astrocytomas.


Assuntos
Astrocitoma/genética , Neoplasias Encefálicas/genética , DNA de Neoplasias/análise , Lobo Frontal , Glioblastoma/genética , Região Organizadora do Nucléolo , Aneuploidia , Antígenos Nucleares , Astrocitoma/imunologia , Neoplasias Encefálicas/imunologia , DNA de Neoplasias/genética , Glioblastoma/imunologia , Humanos , Proteínas Nucleares/análise , Prognóstico
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