Slit Skin Smear (SSS) Introduction
Slit Skin Smear (SSS) is a very useful technique to see the presence of the causative organism, Mycobacterium leprae, in the skin smear of a patient’s body since slit skin smear (SSS) is a gold standard technique for the leprosy diagnosis.
The causative agent of leprosy, also called Hansen’ disease is M. leprae and three cardinal signs of leprosy are as follows-
- Hypo or hyperpigmented anaesthetic patch
- Peripheral nerve involvement
- Positive Acid-Fast Bacilli (AFB)in slit skin smear
- In 1963, Wade introduced the SSS method to diagnose leprosy.
- A small amount of bloodless tissue fluid by slit and scrape method
- Cheap and easy to perform
Slit Skin Smear (SSS) Preparation
Requirements for Slit Skin Smear (SSS)
- Surgical Blade No. 15
- Surgical Handle No. 3
- Clean and grease-free glass slides
- Spirit swab
- Spirit lamp
- Swab stick
- Dry cotton
- Tincture of benzoin
- Matchbox
- Slide box
- Diamond pencil
- Forceps
- Gloves
Procedure of Slit Skin Smear
- Carefully explain the procedure to the patient.
- Prepare clean micro slide.
- Adequately clean sites with spirit swabs.
- Pinch area to make bloodless.
- Cut 5 mm long and 2 mm deep only.
- Scrape bloodless tissue fluid.
- Spread fluid evenly making approximately 8 mm diameter round smear on the slide.
- Make one slide per patient i.e., four smears per slide, one site – one smear (Note- Make sure that you maintain the same sequence of smears on the slide.)
- Air dry and fix over spirit-lamp; store in a dry place.
- Cover the cut site with a tincture of benzoin and apply a pinch of cotton.
Staining of Slit Skin Smear (SSS)
Ziehl-Neelsen (ZN) Method
Requirements for Staining
- Staining Rack
- Spirit lamp
- Stain droppers
- Stains:
- 1% carbol fuchsin (freshly prepared)
- 1% acid alcohol or 5% sulfuric acid
- 1% methylene blue
- Slide drying rack
- Specimens: It depends on the form of leprosy suspected by the treating physician; the preferred specimens may be. 1. Slit Skin smears from the earlobes, elbows, and knees2. Skin biopsy from edges of active patches3. Nerve biopsy from thickened nerves
Procedure of Staining
- Set staining rack over lab sink.
- Align the slides on the staining rack.
- Cover slides with 1% carbol fuchsin and heat gently for 15 minutes.
- Wash slides with tap water.
- Decolorize slides with 1% acid alcohol (HCl in 70 % Alcohol) for few seconds or 5% Sulphuric Acid solution for 10 seconds.
- Wash slides once more with tap water.
- Cover the slides with 1% methylene blue for 1 minute.
- Wash slides once more with tap water.
- Air dry slides on the drying rack.
Observation of Slit Skin Smear
- Scan under 10X objective of a microscope.
- Finally, observe under 100X objective (oil immersion).
- Read slide systematically in a zigzag fashion.
- Each smear is graded according to Ridley’s logarithmic scale as shown below.
Result Interpretaion of Slit Skin Smear
Grading: Ridley’s logarithmic scale
0 = Negative; no AFB in entire smear
1+ = 1-10 AFB in 100 microscopic field
2+ = 1-10 AFB in 10 microscopic field
3+ = 1-10 AFB in 1 average microscopic field
4+ = 10-100 AFB in 1 average field
5+ = 100-1000 AFB in on average field
6+ = >1000 AFB, AFB in 1 average field with clumps (globi)
Bacteriological Index (BI)
- An estimation of the number of bacilli in the smear; semi-quantitative method (Ridley 1958)
- BI is calculated by adding the index from the various sites and divided by the total number of sites examined
- Maximum BI- site is also indicated inpatient report
Morphological Index (MI)
- An estimation of solidly stained bacilli in a smear
- Count 200 AFB of all morphology and note only solidly stained bacilli among them
- Expressed in Percentage.
- When bacilli are <200, expressed infraction
- Characteristics of Solid bacilli:
- Uniformly stained organism
- Round ends
- Length is approximately 5 x width
- Parallel sides
Applications of Slit Skin Smear (SSS)
- To diagnose: All leprosy cases does not show positive to M. leprae (10-50%)
- To classify the disease whether multibacillary (MB) or paucibacillary (PB)
- Smear positive cases are MB
- It shows highly positive in LL/BL and weakly/negative in BB/BT cases
- ≥ 4+ at any individual site is treated with 24 months MB-multidrug therapy (MDT) in a referral center
- To monitor the efficacy of treatment
- To rule out relapse
- To have an idea of drug resistance
Limitations of Slit-Skin Smear
- SSS sensitivity is low toward the tuberculoid pole and thus PB cases of leprosy can be missed.
- A negative SSS does not exclude leprosy since it requires a minimum of 10,000 bacilli/g of tissue for reliable detection by Z- N staining.
- Smears may be negative in PB leprosy lesions where M. leprae load is scanty.
- It is a technician-dependent test and hence a skilled staff needs.
- The observations are also subjective.
Keynotes on SSS
- SSS has even been low sensitivity (10–50%, depending upon the expertise of laboratory workers), It is still the gold standard for all diagnostic techniques due to specificity of nearly 100%.
- Molecular test, PCR assay has been increasingly used as an alternative for its diagnosis due to its higher sensitivity.
- The sensitivity of the PCR is higher in the multibacillary patients due to have of a load of bacilli.
- The difference between SSS and Fite Faraco methods are as follow-SSS detects AFB in smear taken from dermis and the Fite Faraco method detects AFB in tissue obtained by skin biopsy taken from clinically suspected lesions.
- Four common sites for slit skin smears are -Right ear-lobeLeft ear-lobeEdge of the active lesion (if no skin lesion right arm)Edge of the active lesion (if no skin lesion right thigh)
- Follow up: Smear is always performed from previous smear site
- If any new skin lesion also takes from the edge of the lesion.
- SSS smear interpretation-Bacilli are red dots against a blue background whereas viable bacilli are seen as uniformly stained bacilli or solid bacilli having length 4 times greater than the breadth. Bacilli sides are parallel and the ends may be rounded, straight, or pointed. The dead bacilli ( M. leprae) stain irregularly and appear as granular or fragmented. The bacilli may be seen singly, in small groups, or closely packed bunches called globi (as shown above image). Irregular blue-stained structures scattered among the bacilli are the cells of various structures in the skin.
Further Reading
- https://www.cdc.gov/leprosy/health-care-workers/laboratory-diagnostics.html
- https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5189933/#:~:text=Detection%20of%20Mycobacterium%20leprae%20in,due%20to%20its%20higher%20sensitivity
- https://pubmed.ncbi.nlm.nih.gov/22097999/
- https://www.jcdr.net/article_fulltext.asp?issn=0973-709x&year=2020&month=March&volume=14&issue=3&page=WC01&id=13543
- https://leprosyreview.org
- https://onlinelibrary.wiley.com/doi/abs/10.1111/j.1365-4362.1990.tb03746.x
- https://www.ijpd.in/article.asp?issn=2319-7250;year=2019;volume=20;issue=4;spage=341;epage=344;aulast=Gautam