prompt1 : extract information from  breast pathology report. List the histological classification, i.e. type of cancer or DCIS, subtype, description of any necrosis, any mention of tumor infiltrating lymphocytes,  histological grade, nuclear grade,  lymphovascular invasion, calcification, receptor status, IHC and any other ancillary testing results.  List out and expand the main points.
prompt2 : The report is - Subtype LumA, P.22/33. BIAGNOSIS: AREAST. LEFT. BOTAL MASTECTOMY -. COBULAR NEOPLASIA (ATYPICAL LOBULAR HYPERPLASIA) (sec comment). B. FIBROADENOMÀ, DUCTAL EPITHELIAL HYPERPLASIA, FIBROCYSTIC CHANGE. C. SKIN AND NIPPLE, NO TUMOR SEEN. PART 2: BREAST, RIGHT, TOTAL MASTECTOMY -. A. INFILTRATING DUCTAL CARCINOMA, NOS TYPE, MODERATELY DIFFERENTIATED. 8. THE TUMOR IS MULTIFOCAL, MULTICENTRIC, LOCATED AT THE JUNCTION OF UPPER OUTER QUADRANT. (UOQ) AND UPPER INNER QUADRANT (UIO) AS WELL AS IN THE UPPER OUTER QUADRANT (UOO). c. THE TUMOR NODULES MEASURE 2.5 CM (GROSS MEASUREMENT) AND 0.5 CM (MICROSCOPIC. MEASUREMENT) RESPECTIVELY. D. NOTTINGHAM SCORE 6/9 (TUBULES 2. NUCLEAR GRADE 2, MITOSIS 2),OVERALL GRADE 2/3. E. NO DEFINITIVE LYMPHOVASCULAR INVASION IS IDENTIFIED. F. DUCTAL CARCINOMA IN 8ITU, SOLID TYPE WITH COMEDO NECROSIS, NUCLEAR GRADE 3 WITH. LOBULAR EXTENSION, COMPRISING 25% OF THE TOTAL TUMOR VOLUME AND IS PRESENT IN. ASSOCIATION AND AWAY FROM THE INVASIVE CARCINOMA. G. MARGIN3: DEEP AND ANTERIOR MARGISN OF RESECTION ARE FREE OF INVASIVE AS WELL AS IN SITU. CARCINOMA, CLOSEST ANTERIOR MARGIN IS 7MM AWAY. K. ATYPICAL DUCTAL HYPERPLASIA. PREVIOUS BIOPSY SITE CHANGES (I/1 AND #2), ( 3EC COMMENT-2). I. FIBROADENOMA, PSEUDOANGIOMATOUS STROMAL HYPERFLASIA (PASH), COLUMNAR CELL CHANGE. J. SKIN AND NIPPLE, NO TUMOR SEEN. K. ER-POSITIVE, PR-POSITIVE. MER 2/NEU -STRONGLY POSITIVE (IHC 3+ AS WELL AS FISH-AMPLIFICATION),. CROSS REFER. PART 3: #1 SENTINEL LYMPH NODE, RIGHT AXILLA, BIOPSY-. ONE LYMPH NODE WITH METASTATIC CARCINOMA, THE METASTATIC FOCUS MEASURES 6MM (ON GLASS. SLIDE) FOCAL EXTRACAPSULAR EXTENSION IS IDENTIFIED (1/1). PART 4: #2 SENTINEL LYMPH NODE, RIGHT AXILLA, BIOPSY. ONE BENIGN LYMPH NODE, NO TUMOR SEEN (0/1). PART 5: #3 SENTINEL LYMPH NODE, RIGHT AXILLA, BIOPSY -. ONE BENIGN LYMPM NOPE, NO TUMOR SEEN (0/1). PART 6: #4 SENTINEL LYMPH NODE, RIGHT AXILLA, BIOPSY -. ONE BENIGN LYMPH NODE, NO TUMOR SEEN (0/1). PART 7: NON-SENTINEL LYMPH NODE, RIGHT AXILLA, BIOPSY-. ONE BENIGN LYMPH NODE, NO TUMOR SEEN (0/1). LATERALITY: SYNOPTIC - PRIMARY INVASIVE CARCINOMA OF BREAST. PROCEDURE: Right. Simple mastactoiny. Upper outer quacrant. SIZE OF TUMOR: Upper inner quadrant. MULTICENTRICTYMOUTIFOCAUTY OF Maximum INVASIVE dimension FOCI: Invasivo component: , 5 on. TUMOR AGGREGATE SIZE: TUMOR TYPE (invasivo component): Sum of the sizes of multiple invasive tumors: 3.0 cm. NOTTINGHAM SCORE: Ductal adenocamino, NOS. Nuclear grade: 2. Tubule formation 2. Milorie activily 2. total Nottingham score: G. ANO|OLYMPHATIC INVASION: No Nottingham grade (1. 2, 3): 2. DERMAL LYMPHATIC INVASION: CALCIFICATION: TUMOR TYPE, IN SITU: Yes, malignant zonea. Solid. Comedo. SURGICAL MARGINS INVOLVED By INVASIVE of COMPONENT: tumor occupied by In situ component: 25 %. Percent DCIS admixed und outsino of Invasivo carcinoma component. SURG MARGINS INVOLVED BY IN SITU No COMPONENT: PAGET'S DISEASE OF NIPPLE: LYMPH NODES POSITIVE: LYMPH NODES EXAMINED: 1. METHOD(S) OF LYMPH NODE EXAMINATION: 4. Discrepancy. SENTINEL NODE METASTASIS: H/E stain. ONLY KERATIN POSITIVE CELLS ARE Yes PRESENT: initials Mittory. CUALI,. SIZE OF NODAL METASTASES: LYMPH NODE META8TASIS(-ES) WITH Diameter EXTRACAPSULAR of targest lymph EXTENSION: node motestasis: 8 mm. METASTASES TO IPSILATERAL INTERNAL No Yes MAMMARY LYMPH NODE (IF APPLICABLE): T STAGE, PATHOLOCIC. SKIN INVOLVED (ULCERATION): N STAGE, PATHOLOGIC-. p12. M STAGE, PATHOLOGIC: pN1. ESTROGEN RECEPTORS. pMX. poritive. PROGESTERONE RECEPTORS: HER2/NEU: positive. 3+.

expanded version (tokens=1722) : 
 Based on the breast pathology report, the following information can be extracted:

1. Histological classification: The report indicates the presence of multiple conditions in both breasts, including lobular hyperplasia, fibroadenoma, ductal epithelial hyperplasia, fibrocystic change, and infiltrating ductal carcinoma.

2. Subtype: The infiltrating ductal carcinoma is of the Luminal A subtype.

3. Necrosis: The report mentions comedo necrosis in association with some of the ductal carcinoma.

4. Tumor infiltrating lymphocytes: The report does not mention the presence of tumor-infiltrating lymphocytes.

5. Histological grade: The infiltrating ductal carcinoma is graded as moderately differentiated (grade 2 out of 3), based on the Nottingham score.

6. Nuclear grade: The nuclear grade of the infiltrating ductal carcinoma is 2, according to the Nottingham score.

7. Lymphovascular invasion: There is no definitive evidence of lymphovascular invasion, according to the report.

8. Calcification: The report indicates the presence of calcification within the malignant zones.

9. Receptor status: The infiltrating ductal carcinoma is ER-positive, PR-positive and HER2/neu strongly positive.

10. IHC and other ancillary testing results: The report indicates that the HER2/neu receptor status was confirmed with both IHC and FISH testing. The report also mentions the presence of atypical ductal hyper

prompt : Please generate a succinct report in 75 words from the above information. Exclude any filler words or sentences. If something is not mentioned or specified, exclude it from the report. Low verbosity.

final output (tokens=1895) : 
 The breast pathology report identifies the presence of lobular hyperplasia, fibroadenoma, ductal epithelial hyperplasia, fibrocystic change and infiltrating ductal carcinoma that is Luminal A subtype. Necrosis is present in association with some of the ductal carcinoma, while no lymphovascular invasion is identified. The tumor is 2.5 cm in size and moderately differentiated with a nuclear grade of 2. HER2/neu status indicates strong positivity by both IHC and FISH testing. No Paget's disease or metastases are seen and surgical margins are free of invasive carcinoma.

