1. بسم الله الرحمن الرحيم Department of Pathology College of Medicine
Introduction ,Tissue processing & sectioning
Professor Dr. Wahda M.T.Al-Nuaimy
Department of Pathology
College of Medicine
University of Mosul
4th October 2015

2. Pathology
pathology is the study (logoy) of suffering (patho).
Pathology: is the branch of medical science that studies the causes, nature and effects of diseases“
Disease: any abnormality in the structure and/or function of an organ or tissue.
Branches of pathology
Genetic Hematology ,Histopathology , Microbiology , Biochemistry and Cytology

3. Biopsy: examination of tissue taken from living body: gross (macroscopical) & microscopical examination).
Autopsy
Also known as a post-mortem examination .
Is a procedure that consists of a thorough examination of a dead body to determine the cause and manner of death and to evaluate any disease or injury that may be present.

4. Types of biopsy
Incisional biopsy: a portion of tissue from a large lesion is taken-only diagnostic
Excisional biopsy: the entire lesion is removed with a margin of adjacent normal tissue-diagnostic & therapeutic.
Punch biopsy: by biopsy forceps in the uterus ,cervix, oral cavity, esophagus.

7. 4) Core needle biopsy: by wide bore needle used percutaneously for sampling of internal organs.
5) Curettage biopsy : for diagnosis of internal diseases e.g. D&C for uterus to diagnosis abnormal uterine bleeding.

8. Handling of biopsy:
Once a biopsy is taken, it should be put in plastic or metal container with adequate amount of fixative ( 10% formalin) which causes rapid denaturation of cellular proteins & prevents autolysis. It should be sent to the lab with a request form including patient’ s name, age, sex, short clinical notes, type of biopsy, name of tissue submitted & findings of operation.

9. Gross examination

10. General principles for gross examination:
Proper identification & orientation of the specimen.
Place the specimen on a cutting board & record all the following data
Type of specimen
Dimension ( in centimeters)
Weight
Shape
Consistency
Surgical margins whether included or not involved by the tumor.

11. Histopathological techniques
Deals with tissue with preparation of tissue for histopathological examination, the aim of these technique is to preserve microscopic anatomy of tissues & to cut tissue in very thin sections( 4-5 microns) this is achieved by passing tissue in a series of process.

13. Fixation. Dehydration. Cleaning. Embedding. Cutting. Staining.
Tissue processing can be done manually or mechanically & includes the following processes
Fixation.
Dehydration.
Cleaning.
Embedding.
Cutting.
Staining.

15. 1- Fixation
Most fixatives act by denaturating or precipitating cellular proteins which form meshwork that hold other structures & prevent autolysis.
The most widely used fixative is 10% formalin.

16. 2- Dehydration 3- Cleaning
Is removal of water molecules from tissues and is achieved by graded alcohol.
3- Cleaning
Alcohol replace water in the tissues, removal of alcohol from tissues is by Xylene which creates empty tissue spaces to be infiltrated by wax.

17. 4- Embedding with wax
Paraffin wax is used for embedding of tissue which form tissue blocks after cooling. it can be trimmed into thin sections (4-5microns) using the microtom the sections are placed on glass slides and become ready for staining.

25. Hematoxylin & Eosin (H&E) is the most widely used stain in histopathology .It’s the corner stone stain in histology.
Nuclei appear dark blue.
Collage & cytoplasm appear pink.
Keratin appears pink to red.

32. Special stains PAS ( periodic acid schiff) stain glycogen & mucin .
Congo-red for amyloid.
Sudan-black for fat.
Gimsa stain for Helicobacter pylori.
Tuludine blue stain for mast cells.

33. H. pylori stained dark blue with Gimsa stain

34. Amyloid deposits stain orange-red with Congo Red stain

35. Cytology: is the study of normal & abnormal morphologic characteristics of human cells. Samples could be ;fluid cytology , Pap smear from the uterine cervix , FNAC , scraping of the lesion.

36. Frozen section
In this technique the tissue is frozen rapidly (using cryostat) to -20ºC ten sections are cut and stained (without passing in the steps of tissue processing) so that tissue can be examined microscopically within 5-10 minutes of removal from the body.

37. It allows rapid diagnosis of the nature of the lesion whether benign or malignant to decide the next step in surgery e.g. in breast mass whether lumpectomy in bengin mass or mastectomy in malignant mass.
All laboratory staff should be informed and all preparations should be completed before arrival of tissue.

38. Thank You