Diagnostic Accuracy of Cd1a Immuno Histochemical Evaluation in Comparison with H & E and Giemsa for Cutaneous Leishmaniasis
DOI:
https://doi.org/10.61919/jhrr.v3i2.272Keywords:
Cutaneous leishmaniasis, CD1a immunohistochemical staining, Hematoxylin and Eosin, Giemsa, histopathological diagnosis, Leishmania amastigotesAbstract
Background: Cutaneous leishmaniasis remains a global health challenge, with diagnosis largely dependent on the visualization of Leishmania parasites in infected tissue. Traditional staining methods, such as Hematoxylin and Eosin (H&E) and Giemsa, have been the cornerstone of histopathological diagnosis, but they come with limitations in sensitivity and specificity.
Objective: This study aimed to evaluate the diagnostic accuracy of CD1a immunohistochemical staining in the detection of leishmania amastigotes in skin biopsies and compare its efficacy with H&E and Giemsa staining methods.
Methods: A total of 110 skin biopsy samples with a strong clinical suspicion of cutaneous leishmaniasis were examined using H&E, Giemsa, and CD1a immunohistochemical staining techniques. The sensitivity and specificity of these methods were analyzed and compared to ascertain the most effective diagnostic approach.
Results: The study identified leishmania amastigotes in 78% of the cases using H&E staining, while Giemsa staining resulted in amastigote detection in 82% of cases. Notably, CD1a immunohistochemical staining showed a remarkable sensitivity, identifying amastigotes in 95% of the samples. The increase in detection rate with CD1a staining was statistically significant when compared to H&E (p<0.05), with CD1a revealing amastigotes in an additional 23% of cases where H&E staining was negative. Giemsa staining was able to detect amastigotes in three cases that were not visible with H&E, suggesting its potential role as a complementary technique in certain diagnostic scenarios.
Conclusion: The study concludes that CD1a immunohistochemical staining significantly enhances the detection of leishmania amastigotes and should be considered as an adjunct to conventional staining methods in the histopathological diagnosis of cutaneous leishmaniasis. Future diagnostic protocols could benefit from the incorporation of CD1a staining to improve accuracy.
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References
Sundharkrishnan L, North JP. Histopathologic features of cutaneous leishmaniasis and use of CD1a staining for amastigotes in Old World and New World leishmaniasis. Journal of cutaneous pathology. 2017 Dec;44(12):1005-11.
Casanova C, Motoie G, Domingos MD, Silva VG, Silva MD, Galati EA, Galvis-Ovallos F. The transmission of visceral leishmaniasis in the municipality of Guarujá, on the Coast of São Paulo state, Brazil. Revista de Saúde Pública. 2022 Feb 23;56:1.
Kayani B, Sadiq S, Rashid HB, Ahmed N, Mahmood A, Khaliq MS, Maqsood R, Rashid H, Hasan S, Mushtaq MH, Zia UU. Cutaneous Leishmaniasis in Pakistan: a neglected disease needing one health strategy. BMC Infectious Diseases. 2021 Dec;21:1-0.
Masmoudi A, Hariz W, Marrekchi S, Amouri M, Turki H. Old World cutaneous leishmaniasis: diagnosis and treatment. Journal of dermatological case reports. 2013 Jun 6;7(2):31.
Hepburn NC. Cutaneous leishmaniasis. Clinical and experimental dermatology. 2000 Sep 1;25(5):363-70.
Fernandez‐Flores A. A new scenario in the immunohistochemical diagnosis of cutaneous leishmaniasis. Journal of Cutaneous Pathology. 2017 Dec;44(12):1051-2.
Karram S, Loya A, Hamam H, Habib RH, Khalifeh I. Transepidermal elimination in cutaneous leishmaniasis: a multiregional study. Journal of cutaneous pathology. 2012 Apr;39(4):406-12.
Gaspari V, Zaghi I, Macrì G, Patrizi A, Salfi N, Locatelli F, Carra E, Re MC, Varani S. Autochthonous cases of mucosal leishmaniasis in Northeastern Italy: Clinical management and novel treatment approaches. Microorganisms. 2020 Apr 18;8(4):588.
Bamorovat M, Sharifi I, Dabiri S, Shamsi Meymandi S, Karamoozian A, Amiri R, Heshmatkhah A, Borhani Zarandi M, Aflatoonian MR, Sharifi F, Kheirandish R. Major risk factors and histopathological profile of treatment failure, relapse and chronic patients with anthroponotic cutaneous leishmaniasis: a prospective case-control study on treatment outcome and their medical importance. PLoS neglected tropical diseases. 2021 Jan 28;15(1):e0009089.
de Vries HJ, Schallig HD. Cutaneous leishmaniasis: a 2022 updated narrative review into diagnosis and management developments. American Journal of Clinical Dermatology. 2022 Nov;23(6):823-40.
Piyasiri SB, Dewasurendra R, Samaranayake N, Karunaweera N. Diagnostic Tools for Cutaneous Leishmaniasis Caused by Leishmania donovani: A Narrative Review. Diagnostics. 2023 Sep 18;13(18):2989.
Saïdi N, Galaï Y, Ben-Abid M, Boussoffara T, Ben-Sghaier I, Aoun K, Bouratbine A. Imaging Leishmania major antigens in experimentally infected macrophages and dermal scrapings from cutaneous leishmaniasis lesions in Tunisia. Microorganisms. 2022 Jun 4;10(6):1157.
Vega DM, Di Meglio M, del Valle Alonso S, Alvira F, Montanari J. Nanomaterials for Diagnosis, Treatment, and Prevention of Human Cutaneous Leishmaniasis: A Review. OpenNano. 2023 Apr 29:100158.
Singh M, Balhara K, Rana D, Kumar R, Dhankar N, Singh S, Bellichukki P, Paul S, Chartian SM. Lymph Node Cytology: Morphology and Beyond!.
Liersch J, von Köckritz A, Schaller J. Dermatopathology 101: part 1–inflammatory skin diseases. JDDG: Journal der Deutschen Dermatologischen Gesellschaft. 2017 Jan;15(1):9-30.
Gujral S. Pathology Tissues of Lymphoreticular. Hematopathology: Advances in Understanding. 2019 Aug 2:265.
Leach M, Bain BJ. Haematology: From the Image to the Diagnosis. John Wiley & Sons; 2021 Jun 25.
Medeiros LJ, Miranda RN. Diagnostic pathology: Lymph nodes and extranodal lymphomas E-Book. Elsevier Health Sciences; 2017 Jul 12.
Zeppa P, Cozzolino I. Lymph Node FNC: Cytopathology of Lymph Nodes and Extranodal Lymphoproliferative Processes. Karger Medical and Scientific Publishers; 2017 Nov 14.
Brazzell JL, Heinrich D, Walz JZ. Dermal and subcutaneous masses. Veterinary Cytology. 2020 Sep 1:115-37.
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