Professional Documents
Culture Documents
C. Quality Assurance
Quality Assurance in Histopathology and Cytology Section Histopathology record:
A. Checking of Documents Signatories
Specimen handling 6. Shave Biopsy- removing of thin
Turn around time of results Where small fragments of tissue are shaved from a surface
o Surgical pathology and cytopathology: 3-5 days 7. Curreting- curette(instrument used)
o Frozen section: 5-15 minutes Tissue is scooped or spooned to remove tissue or growths from
o Autopsy result: 1 week body cavity such as endometrium or cervical canal.
Storage time
o Specimen: 3-4 weeks to up to 1 year
Methods of Fresh Tissue Examination
o Tissue blocks: 10 years 1. Teasing/Dissociation-
o Slide: indefinitely Aka: Dissection or Separation
o Malignant: whole and tinatanggal NSS or Ringer’s Lactate solution
o Benign: portion lang Examined Stained or unstained
Disadvantage: Anatomical relationship may get destroyed
2. Squash preparation of Crushing- small piece of tissue is less than 1 mm
Methods of tissue preparation for histopathologic study and placed bet. 2 microscopic slide
Slice of tissue must be less than 1mm
A. Fresh Tissue Examination
Tissue is placed bet. 2 slides
Specimen Processed in FTE
Stained with vital stain
1. Fine Needle Aspiration (FNA)- no anesthesia
3. Smearing- used for cytologic studies
Simplest and least invasive method
Streaking: uniform distribution in Zigzag manner
Collection of samples in limps or mass in the body
Spreading- used in thick or mucoid specimen
2. Core Needle Biopsy
Pull apart/ wedge method
Used when large samples is needed
4. Touch preparation or impression smear
Used to diagnose breast abnormalities, prostate issues and various
Surface of freshly cut piece of tissue is brought into contact and
other suspicious masses
pressed on the surface of a clean glass slide
3. Incisional Biopsy
B. Conventional tissue processing
Removal of a small portion of tissue from a larger mass
Described the various steps required to take the tissue from
Results can provide information for treatment planning and
fixation to the state where is completely infiltrated with fixation
further management
to the state where is completely infiltrated with suitable
4. Excisional Biopsy
histological wax and can be embedded for section cutting on the
Removal of entire area affected
microtome
Preferred when suspicious area if malignancy is high
5. Punch Biopsy- comparable to core needle biopsy
Primary technique for obtaining diagnostic full thickness skin
specimens.
Uses a circular blade Steps of Conventional Tissue Processing
1. Fixation of tissues
Process by which the cells or tissues are fixed in chemical and
partly physical state
Results in the denaturation and coagulation of proteins in the
tissue
Aims of fixation-to preserve the tissue as close to their living
state as possible, to prevent tissues from changing their shape
and size during processing, to harden the tissue, to allow clear
staining of sections
Mechanism of Fixation
o Additive fixative
Chemically alter the tissue by bonding with it and
adding themselves to the tissue
Formaldehyde, mercuric chloride, chromium
trioxide, picric acid, glutaraldehyde, osmium
tetroxide and zinc sulfate
o Non-additive fixatives
Act on tissue without chemically combining with
it
Acetone and alcohol