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Cancer (Cancer cytopathology) April 25, 2009;117(2):137-47
Breast fine-needle aspiration samples reported as proliferative breast lesion: Clinical utility of the subcategory proliferative breast lesion with atypia
Chengquan Zhao, MD 1 2 *§, Anwar Raza, MD 1 3, Sue E. Martin, MD, PhD 1, Jiangqiu Pan, MD 1, Timothy S. Greaves, MD 1, Camilla J. Cobb, MD 1 3
1Department of Pathology, Los Angeles County + University of Southern California Medical Center, Los Angeles, California
2Department of Pathology, Magee-Womens Hospital, University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania
3Department of Pathology, Loma Linda University Medical Center, Loma Linda, California
email: Chengquan Zhao (zhaoc@upmc.edu)

*Correspondence to Chengquan Zhao, Department of Pathology, Magee-Womens Hospital, University of Pittsburgh Medical Center, Pittsburgh, PA 15213

Presented at the 96th annual United State and Canadian Academy of Pathology Meeting in San Diego, California, March, 2007.
Fax: (412) 641-1675
§The authors thank Dr. R Marshall Austin (Magee-Womens Hospital, University of Pittsburgh) for his help in reviewing this article.
setDOI("ADOI=10.1002/cncy.20003")

Keywords
atypical proliferative breast lesion • fine-needle aspiration • breast cytology

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. Cancer (Cancer Cytopathol) 2009. © 2009 American Cancer Society.

Received: 28 August 2008; Revised: 13 November 2008; Accepted: 10 December 2008
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本帖最后由 于 2009-04-14 06:22:00 编辑  Figure 2. Three cases of atypical proliferative breast lesions on fine-needle aspiration (FNA) cytology and diagnosed as fibroadenoma on histology specimens and 1 case of fibroadenoma on FNA cytology and histology. (A) A large, loosely cohesive cluster of ductal epithelial cells with nuclear atypia, prominent nucleoli, and rare myoepithelial cells; (B) cluster of ductal epithelial cells with nuclear atypia and rare myoepithelial cells; (C) cellular smear showing many single epithelial cells; (D) FNA cytology of fibroadenoma showing many single myoepithelial cells (A: Papanicolaou stain, original magnification ×400; B-D: Diff-Quick stain, original magnification ×400).

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本帖最后由 于 2009-04-14 06:20:00 编辑  Figure 1. Four cases of atypical proliferative breast lesions on FNA cytology and diagnosed as invasive carcinoma on histology specimens. (A) Small clusters of cells with small, round, and uniform nuclei in a tubular carcinoma case; (B) hypocellular specimen with few clusters of ductal epithelial cells with cytologic atypia in an invasive ductal carcinoma case; (C) one cluster of cells with small, round, and uniform nuclei in an invasive lobular carcinoma case; (D) one very cohesive cluster of ductal epithelial cells with mild cytologic atypia in an invasive ductal carcinoma case (A-D: Papanicolaou stain, original magnification ×400).

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Table 5. Cytologic Features of 99 Fibroadenoma Diagnosed as Proliferative Breast Lesions in Fine-Needle Aspiration

Cytologic Feature Case No.

Stromal component
Present 6
Rare 14
None 79
Honeycomb sheets
Present 69
None 30
Antler horn clusters
Present 16
None 83
Cellularity
Low 38
Moderate 40
High 21
Atypia
Mild 30
Moderate 12
None 57
Myoepithelial cells
Present 70
Rare or none 29
Complex sheet
Present 57
None 42
Clusters of ductal cell w/o myoepithelial cells
Present 86
None 13
Discohesive clusters
Present 63
Absent 16

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Table 6. Usual Ductal Hyperplasia in Surgical Specimens of 99 Fibroadenomas

Degree No. %

None 10 10.1
Mild 16 16.2
Moderate 42 42.4
Marked 31 31.3

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Table 3. Cytologic Features of 15 Invasive Breast Carcinomas

Cytologic Features Case No.

Cellularity
Low 13
Moderate 2
High 0
Cytologic atypia
Mild 7
Moderate 8
Marked 0
Myoepithelial cells
Present 6
Rare 6
Absent 3
Monocell population
Present 9
No 6
Complex fragments
Present 8
Absent 7
Cluster w/o myoepithelial cells
Present 15
Absent 0
Single epithelial cell
Present 10
Absent 5
Discohesive clusters
Present 11
Absent 4

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Table 4. Surgical Features of 15 Invasive Carcinomas

Ductal carcinoma in situ present No. (%)

Invasive ductal carcinoma 6/8 (75)
All other carcinoma 0/7 (0)
Lobular carcinoma in situ present
Invasive lobular carcinoma 2/5 (40)
All other carcinomas 0/10
Nottingham total score
4 3 (20.0)
5 5 (33.3)
6 7 (46.7)
Nottingham grade
1 8 (53.3)
2 7 (46.7)
3 0

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Table 1. Patients' Ages and Tumor Sizes

Groups Mean Age (range) P* Mean Size, cm (range) P*

Total, 172 cases 39.4 (14-68) 2.1 (.5-10)
Proliferative breast lesion without atypia, 120 cases 37.4 (14-67) 1.9 (.5-8)
Atypical proliferative breast lesion, 52 cases 44.4 (25-68) .003 2.7 (1-10) <.001
FA: Cytology of proliferative breast lesion without atypia, 83 cases 34.7 (14-55) 1.9 (.5-6)
FA: Cytology of atypical proliferative breast lesion, 16 cases 39.2 (25-50) .048 2.4 (1-10) .176
FA, total 99 cases 35.4 (14-55) 2.0 (.5-10)
Malignancy, 21 cases 48.2 (28-68) <0.001 3.3 (1.5-6) <.001

   FA indicates fibroadenoma.
  * The P value was derived from the Student t Test.
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Table 2. Correlation of Cytologic and Histologic Diagnosis in 172 Patients With Proliferative Breast Lesions

Histology No. of Cases (%) Atypical Proliferative Breast Lesion (%) Proliferative Breast Lesion Without Atypia (%)

Malignant 21 (12.2) 19 (36.5) 2 (1.7)
Invasive ductal carcinoma 8 (4.6) 6 (11.5) 2 (1.7)
Invasive lobular carcinoma 5 (2.9) 5 (9.6) 0
Invasive mucinous carcinoma 1 (.6) 1 (1.9) 0
Invasive tubular carcinoma 1 (.6) 1 (1.9) 0
Phyllodes tumor, malignant 1 (.6) 1 (1.9) 0
Ductal carcinoma in situ 5 (2.9) 5 (9.6) 0
Benign* 151 (87.8) 33 (63.5) 118 (98.3)
Fibroadenoma 99 (57.6) 16 (30.8) 83 (69.2)
Fibrocystic change/usual ductal hyperplasia 12 (7.0) 0 12 (10)
Intraductal papilloma 4 (7.7) 4 (7.7) 4 (3.3)
Adenomyoepithelioma 5 (2.9) 0 5 (4.2)
Fibrosis with usual ductal hyperplasia 5 (2.9) 0 5 (4.2)
Gynecomastia 4 (2.3) 4 (7.7) 0
Sclerosing adenosis 4 (2.3) 0 4 (3.3)
Tubular adenoma 3 (1.7) 2 (3.9) 1 (.8)
Atypical ductal hyperplasia 3 (1.7) 2 (3.9) 1 (.8)
Atypical papilloma 3 (1.7) 3 (5.8) 0
Atypical lobular hyperplasia 2 (1.2) 1 (1.9) 1 (.8)
Phyllodes tumor, benign 2 (1.2) 0 2 (1.7)
Granulomatous mastitis 1 (.6) 1 (1.9) 0
Total 172 52 (30.2) 120 (69.8)

  * Including a few cases of atypical ductal hyperplasia and atypical lobular hyperplasia.
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