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1.
Cancer ; 117(2): 137-47, 2009 Apr 25.
Article in English | MEDLINE | ID: mdl-19365832

ABSTRACT

BACKGROUND: The fine-needle aspiration (FNA) diagnosis of proliferative breast lesion is an indeterminate category. The aim of this correlative study was to determine whether a subcategory of "proliferative breast lesion with atypia" was achievable and whether this subcategory has management utility. METHODS: Breast FNA cases from 2000 through 2005 diagnosed as proliferative breast lesion and proliferative breast lesion with atypia were retrieved. Both cytologic and surgical slides of these cases were reviewed blindly. A cytologic diagnosis of proliferative breast lesion (without atypia) or proliferative breast lesion with atypia was used if the findings of the proliferative breast lesion did not fit a more specific category. RESULTS: Of the 3934 breast FNAs performed on palpable breast masses from January 2000 to December 2005 at the LAC + USC Medical Center, 317 (8.1%) were diagnosed cytologically as proliferative breast lesion with atypia, without atypia or without mention of atypia. There was subsequent histopathology on 201 of these cases. After the cytologic smears were reviewed, 29 cases were excluded from this study. Of the 172 remaining cases, 21 (12.2%) were found to be malignant and the remaining 151 (87.8%) were found to be benign on histology. Of the malignant cases, 90% had an FNA diagnosis of proliferative breast lesion with atypia; of the benign cases, 78% were interpreted as proliferative breast lesion without atypia. CONCLUSIONS: Proliferative breast lesion with atypia was clinically significant because it was associated with a significantly increased likelihood of malignancy compared with proliferative breast lesion without atypia. Most of the malignancies had hypocellularity or low nuclear grade on the FNA smears. Fibroadenoma accounted for most of the benign lesions in both proliferative breast lesion and proliferative breast lesion with atypia.


Subject(s)
Breast Diseases/classification , Breast Diseases/pathology , Breast/pathology , Adolescent , Adult , Aged , Biopsy, Fine-Needle , Breast Neoplasms/classification , Breast Neoplasms/pathology , Child , Cytodiagnosis/methods , Diagnosis, Differential , Female , Humans , Hyperplasia , Middle Aged , Precancerous Conditions/classification , Precancerous Conditions/pathology , Young Adult
2.
Mar Drugs ; 7(1): 9-18, 2009.
Article in English | MEDLINE | ID: mdl-19370167

ABSTRACT

To investigate the protective effects of squid ink in chemotherapy, BALB/c mice were used as animal models of injuries induced by cyclophosphamine, a well known chemotherapeutic drug. The mice were randomly divided into five groups with the same number of males and females in each group. At the end of the experiment, animals were sacrificed to investigate organ indexes and antioxidant ability of the spleen, peripheral blood profile and quantities of bone marrow nucleated cells. Results showed that the hemopoietic function of mice was injured by cyclophosphamine, as indicated by decreases of contents of erythrocytes, leukocytes, hemoglobin and bone marrow nucleated cells (P<0.01), while platelets were not affected (P>0.05), as well as modification of organ indexes (P<0.05) and spleen antioxidant ability (P<0.05 or P<0.01), whereas sepia extract markedly increased the levels of erythrocytes, leukocytes, hemoglobin and bone marrow nucleated cells (P<0.01), but not platelets (P>0.05), and reversed the effects of cyclophosphamine on organ indexes and antioxidant ability of spleen (P<0.01 or P<0.05). In addition, squid ink extract did not change marrow hemopoiesis but improved the antioxidant ability of spleen in the animals. The data suggest that squid ink extract can protect the hemopoietic system from chemotherapeutic injury and could be employed to develop cell-protective drugs for use in clinical treatment of tumours.


Subject(s)
Antioxidants/chemistry , Biological Products/chemistry , Cyclophosphamide/adverse effects , Hematopoiesis/drug effects , Hematopoietic System/drug effects , Sepia/chemistry , Animals , Antioxidants/therapeutic use , Biological Products/therapeutic use , Blood Cell Count , Blood Cells/cytology , Blood Cells/drug effects , Bone Marrow Cells/cytology , Bone Marrow Cells/drug effects , Cytoprotection , Dose-Response Relationship, Drug , Female , Hematopoietic System/cytology , Hemoglobins/analysis , Male , Mice , Mice, Inbred BALB C , Random Allocation , Spleen/cytology , Spleen/drug effects , Spleen/metabolism
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