Tzanck test

Tzanck test
A positive Tzanck test, showing three multinucleated giant cells ("Tzanck cells") in center.
Purpose	diagnosis of varicella-zoster virus and herpes

In dermatopathology, the Tzanck test, also Tzanck smear, is scraping of an ulcer base to look for Tzanck cells. It is sometimes also called the chickenpox skin test and the herpes skin test. It is a simple, low-cost, and rapid office based test. ^[1]

Tzanck cells (acantholytic cells) are found in:

• Herpes simplex ^[2]
• Varicella and herpes zoster
• Pemphigus vulgaris
• Cytomegalovirus

Arnault Tzanck did the first cytological examinations in order to diagnose skin diseases. ^[3] To diagnose pemphigus, he identified acantholytic cells, and to diagnose of herpetic infections he identified multinucleated giant cells and acantholytic cells. He extended his cytologic findings to certain skin tumors as well.

Even though cytological examination can provide rapid and reliable diagnosis for many skin diseases, its use is limited to a few diseases. In endemic regions, Tzanck test is used to diagnose leishmaniasis and leprosy. For other regions, Tzanck test is mainly used to diagnose pemphigus and herpetic infections. Some clinics use biopsies even for herpetic infections. ^[4] This is because the advantages of this test are not well known, and the main textbooks of dermatopathology do not include dedicated sections for cytology or Tzanck smear. ^[5] A deep learning model called TzanckNet has been developed to lower the experience barrier needed to use this test. ^[6]

Procedure

1. Unroof vesicle and scrape base w/ sterile №15 scalpel blade
2. Smear with cotton stick onto a clean glass slide
3. Fix w/ gentle heat or air dry
4. Fix w/ MeOH (Methanol)
5. Stain w/ Giemsa, methylene blue or Wright’s stain.
6. Microscopic examination using an oil immersion lens. (Look for multinucleated giant cells) ^[7]

A modified test can be performed using proprietary agents which requires fewer steps and allows the sample to be fixed quicker.

Cytologic findings

For microscopic evaluation, samples are first scanned with low magnification objectives (X4 and X10) and then examined in detail with the high magnification objective (X100). The X4 objectives are used to select the areas to investigate in detail and to detect some ectoparasites, but the basis of the cytological diagnostic process is the X10 objective. With X10 magnification, the individual characteristics of the cells, the relationship of the cells to each other and the presence of some infection and infestation agents are evaluated. For this reason, most of the cytological examination is spent at this magnification, and most samples are diagnosed at this magnification. The key cytological findings that are observed at low magnification or, in other words, should be investigated according to the clinical characteristics of the patient are as follows: acantholytic cells, tadpole cells, granulomatous inflammation, infectious agents and increases in specific cells.

Major indications, cytologic findings and diagnostic value of Tzanck smear test ^[8]

Diseases			Cytologic findings	Diagnostic value
I. Cutaneous infections
	Bacterial infections
		Bullous impetigo	Dyskeratotic acantholytic cells, abundant neutrophils and clusters of cocci	92% sensitive and 100% specific
		Staphylococcal scalded skin syndrome (SSSS)	Dyskeratotic acantholytic cells, absence of abundant neutrophils and cocci	A Tzanck smear may be a rapid test to distinguish toxic epidermal necrolysis from SSSS
		Mycobacterial infections	Negative images of mycobacteriae, acid-fast bacilli	Maximum acid-fast bacilli positivity (94%) in cases showing caseation necrosis with or without granulomas
		Bacillary angiomatosis	Clumps of coccobacilli of B Henselae in Warthin-Starry-stained smears
	Fungal infections
		Dermatophytic infections	Hyphae and spores
		Candidiasis	Pseudohyphae and spores	Pseudohyphae and spores in 90% of patients with candida folliculitis
		Aspergillosis	Septate hyphae with 45-degree angle branching and/or aspergillus heads
		Blastomycosis	Broad-based budding spores	57.7 - 93% sensitive
		Sporotrichosis	Spherical, oval or cigar-shaped yeasts and asteroid bodies	84.9% sensitive and 57.9% specific
	Viral infections
		Herpetic infections	Acantholytic cells, multinucleated giant cells and eosinophilic inclusion bodies	53.1 - 86% sensitive and 100% specific
		Hand, foot and mouth disease	Syncytial nuclei, absence of acantholytic cells1	72% sensitive and 100% specific
		Human papillomavirus infections	Koilocytes	75% sensitive and 100% specific
		Molluscum contagiosum	Intracytoplasmic inclusion bodies (“Henderson-Patterson’s bodies”)
		Milker’s nodule and orf	Intracytoplasmic inclusion bodies (“Guarnieri’s bodies”)
	Parasitic infections
		Leishmaniasis	Ellipsoid-shaped Leishman-Donovan bodie	30 - 82.6% sensitive and 100% specific
		Demodicosis	More than 5 Demodex mites/cm2	The diagnostic value of cytology for diagnosing Demodex folliculitis is higher than that of histopathology. The sensitivity of histopathology is 60%, whereas that of cytology is 93.3%
		Cutaneous amoebiasis	Trophozoites of Entamoeba histolytica	Direct specimens or PAS and acid phosphatase-stained specimens in cases with doubtful direct specimens show trophozoites of Entamoeba histolytica
II. Immunobullous disorders
	Pemphigus		Acantholytic cells with direct immunofluorescence positivity	With the use of direct immunofluorescence examination, the specificity of cytology for diagnosing pemphigus can be increased from 43% to 100%.
	Erythema multiforme, Toxic epidermal necrolysis		Apoptotic and necrotic cells, absence of acantholytic cells	A Tzanck smear may be a rapid test to distinguish toxic epidermal necrolysis from SSSS
III. Genodermatoses
	Hailey-Hailey disease		Acantholytic cells without direct immunofluorescence positivity	Direct immunofluorescence examination should be made for differentiation from pemphigus.
	Darier’s disease		Acantholytic cells, corps ronds, grains
IV. Spongiotic dermatitis			Presence of more than 10 tadpole cells at x100 magnification
	Contact dermatitis		Tadpole cells and lymphocytes	83% sensitive and 100% specific
V. Granulomatous diseases			Granuloma formation and multinucleated giant cells	The main purpose of cytological examination in granulomatous dermatitis is to detect infectious agents. Foreign body materials are very specific for foreign body granuloma.
	Granuloma annulare		Palisading granuloma and mucin
	Necrobiosis lipoidica		Palisading granuloma and necrobiotic materials
	Foreign-body granuloma		Foreign body
	Juvenile xanthogranuloma		Touton type giant cells and foamy cells
VI. Tumoral lesions
	Benign tumoral lesions
		Mastocytoma	Abundant mast cells	Tzanck smear test is useful for rapid diagnosis of mastocytoma in children
		Sebaceous hyperplasia	Clusters of sebocytes
		Seborrheic keratosis	Hyperkeratosis and horny cysts	87.5% sensitive and 80.8% specific
		Melanocytic nevi	Dermal and epidermal type nevoid cells	87.5% sensitive and 100% specific
		Eruptive vellus hair cysts	Abundant vellus hairs
	Malignant tumoral lesions		Cellular atypia including mitosis, poikilokaryosis, poikilocytosis, nuclear contour irregularity, prominent nucleoli and nuclear molding
		Basal cell carcinoma	Clusters of basaloid cells	The most common reason to use cytological examination in malignant tumoral diseases is to distinguish basal cell carcinoma from other tumors, such as squamous cell carcinoma and melanoma. Tzanck smear test is 97% sensitivity and 86% specificity for the diagnosis of basal cell carcinoma.
		Squamous cell carcinoma	Cytologic atypia of keratinocytes
		Melanoma	Atypical melanocytes
		Lymphoma	Atypical lymphocytes
		Paget’s disease	Isolated or clusters of Paget’s cells
		Kaposi’s sarcoma	Cigar-shaped spindle cells

Tzanck smear examples

• 
  Acantholytic cell and multinucleated giant cell on a smear taken from a vesicular lesion of herpes simplex infection (May-Grünwald Giemsa x1000).
• 
  Extracellular and intracellular (macrophages) leishmania parasites in a patient with cutaneous leishmaniasis (May-Grünwald Giemsa x1000).
• 
  Acantholytic cells on a smear taken from a patient with pemphigus foliaceus (May-Grünwald Giemsa x1000).
• 
  Tadpole cells on a smear taken from a patient with allergic contact dermatitis (May-Grünwald Giemsa x1000).
• 
  A cluster of basaloid cells on a smear taken from a patient with basal cell carcinoma (May-Grünwald Giemsa x1000).

References

1. Durdu M (2019). Cutaneous Cytology and Tzanck Smear Test. Springer International Publishing. ISBN   978-3-030-10721-5.
2. Folkers E, Oranje AP, Duivenvoorden JN, van der Veen JP, Rijlaarsdam JU, Emsbroek JA (August 1988). "Tzanck smear in diagnosing genital herpes". Genitourinary Medicine. 64 (4): 249–54. doi:10.1136/sti.64.4.249. PMC   1194227 . PMID   3169755.
3. Tzanck A (1947). "Le cyto-diagnostic immédiat en dermatologie". Presse Médicale.
4. Horn TD (December 2008). "Commentary: heading the wrong way: the disappearing Tzanck smear". Journal of the American Academy of Dermatology. 59 (6): 965–966. doi:10.1016/j.jaad.2008.08.025. ISSN   1097-6787. PMID   18929430.
5. Kelly B, Shimoni T (2009-06-01). "Reintroducing the Tzanck Smear" . American Journal of Clinical Dermatology. 10 (3): 141–152. doi:10.2165/00128071-200910030-00001. ISSN   1179-1888. PMID   19354329. S2CID   23928319.
6. Noyan MA, Durdu M, Eskiocak AH (2020-10-27). "TzanckNet: A convolutional neural network to identify cells in the cytology of erosive-vesiculobullous diseases". Scientific Reports. 10 (1): 18314. doi:10.1038/s41598-020-75546-z. PMC   7591506 . PMID   33110197.
7. Pettit, Normal Microbiota of the Skin, ATSU School of Osteopathic Medicine Arizona, Lecture Slides. Jan 2013.
8. Durdu M, Seckin D, Baba M (January–February 2011). "The Tzanck Smear Test: Rediscovery of a Practical Diagnostic Tool". Skinmed. 9 (1): 23–32. PMID   21409959 . Retrieved 18 September 2023.

External links

• Tzanck test - medlineplus.org.
• Definition of Tzanck test - medterms.com.