Histopathological spectrum of Pigmented Melanocytic Lesions

Authors

  • Richa Sharma Assistant Professor, Department of Pathology, Santosh Medical College, Ghaziabad, Uttar Pradesh, India
  • Shubhangi Khamankar 2Associate Professor, Department of Pathology, Government Medical College, Gondia, Maharashtra, India
  • Dharitri Bhat Associate Professor, Department of Pathology, Government Medical College, Nagpur, India

Keywords:

Pigmented melanocytic lesions, melanocytic nevi, malignant melanoma, histopathology, skin tumors

Abstract

Background: Pigmented lesions are of a major concern with great psychological impact on quality of life. According to WHO, the
number of melanoma cases worldwide is increasing faster than any other cancer. Pigmented melanocytic lesions encompass a wide
spectrum of benign and malignant entities with overlapping clinical and histopathological features. Accurate histopathological evaluation
remains the gold standard for diagnosis and plays a crucial role in prognostication and therapeutic decision-making.
Methods: This study was carried out in the Department of Pathology of a tertiary care centre in Maharashtra. All the melanocytic lesions
were included in the study.Formalin-fixed, paraffin-embedded tissue sections were processed and stained with hematoxylin and eosin.
Results: A total of 61 cases of pigmented melanocytic lesions were analyzed. Benign melanocytic nevi constituted the majority of
cases, followed by malignant melanoma. The lesions were distributed in the age ranging from 14 - 80 yrs. Male predominance in
seen in cases of melanoma. The most frequently involved anatomical sites were extremities. Malignant melanoma cases demonstrated
characteristic features such as asymmetry, increased mitotic activity, and cytological atypia.
Conclusion: Benign melanocytic nevi are the most common pigmented melanocytic lesions encountered in routine histopathology
practice. Histopathological examination remains indispensable for accurate diagnosis and differentiation between benign and malignant
lesions, thereby guiding appropriate clinical management.

References

Balch CM, Gershenwald JE, Soong SJ, Thompson JF, Atkins

MB, Byrd DR. Final version of 2009 AJCC melanoma staging

and classification. J Clin Oncol. 2009; 27:6199-206.

Mruthyunjayappa S, Mahanthappa H, Gopal MG, Venugopal

SB. A study of spectrum of histopathological features in

patients presenting with hyperpigmented skin lesions. Arch

Med Health Sci. 2016;4(2):189-95

Lens MB, Dawes M. Global perspective of contemporary

epidemiological trends of cutaneous malignant melanoma.

Br J Dermatol 2004;150(2):179- 85

Marsden JR, Newton-Bishop JA, Burrows L, Cook M,

Corrie PG, Cox NH et al. Revised UK guidelines for the

management of cutaneous melanoma 2010. Br J Dermatol

;163(2):238-56.

Cancer Council Australia and Australian Cancer Network.

Clinical Practice Guidelines for the Management of Melanoma

in Australia and New Zealand. New Zealand guidelines group,

Wellington, New Zealand, 2008.

Troxel DB. Medicolegal Aspects of Error in Pathology. Arch

Pathol Lab Med. 2006;130(5):617–19.

Tsai MR, Cheng YH, Chen JS, Sheen YS, Liao YH, Sun

CK. Differential diagnosis of nonmelanoma pigmented skin

lesions based on harmonic generation microscopy. J Biomed

Opt. 2014 Mar;19(3):36001.

Goyal K, Chahal KS, Malhotra SK. To study the

clinicopathological correlation of common pigmentary

disorders of skin. IJSR 2016; 7(4):1448-52.

Gupta P, Karuna V, Grover K, Rathi M, Verma N. The

histopathological spectrum of skin diseases with emphasis on

clinicopathological correlation: A prospective study. IP journal

of Diagnostic pathology and oncology 2018;3(2):91-95

Anand I, Ilanthodi S, Girish P N, Pai MR. A histo-pathological

study with an emphasis on stratification of pigmented lesions

of the skin. Indian J Pathol Oncol 2020;7(4):643-649.

Suvernakar SV, Harwani SR, Deshpande SA.

Clinicopathological Study of Pigmented Skin Lesions. IOSR

journal of Dental and Medical sciences. 2014; 13(5):70-73

Parvathi M, Chowdari B, Lekha GD, Kumar SS, Bhagya

Lakshmi A. A clinico-pathological study of pigmented

cutaneous lesions: a one-year prospective study in a tertiary

care hospital. Int J Res Med Sci. 2017 Dec;5(12):5316-5321.

Laishram RS, Myrthong BG, Laishram S, Shimray R, Kumar

A, Sharma DC. Pigmented skin lesions: are they all of

melanocytic origin? A histopathological perspective. J Pak

Associa Dermatol. 2013;23(3):284-88.

Liu P, Su J, Zheng X, Chen M, Chen X, Li J, Peng C,

Kuang Y and Zhu W (2021) A Clinicopathological Analysis

of Melanocytic Nevi: A Retrospective Series. Front.

Med. 8:681668.

Malladi NSN, Chikhalkar SB, Khopkar U, Kharkar V. A

descriptive observational study on clinical and dermoscopic

features of benign melanocytic neoplasms. Indian J Dermatol

VenereolLeprol. 2020 May-Jun;86(3):251-261.

Scard C, Aubert H, Wargny M, Martin L, Barbarot S. Risk

of melanoma in congenital melanocytic nevi of all sizes:

A systematic review. J EurAcad Dermatol Venereol. 2023

Jan;37(1):32-39.

Patel AB, Kubba R, Kubba A. Clinicopathological correlation

of acquired hyperpigmentary disorders. Ind J Dermatol Ven

Leprol. 2013;79(3): 367-75.

Rice AS, Cook C. Dowling-Degos Disease. [Updated 2023

Aug 16]. In: StatPearls [Internet]. Treasure Island (FL):

StatPearls Publishing; 2025 Jan-. Available from: https://

www.ncbi.nlm.nih.gov/books/NBK531470/

Krüger S, Garbe C, Büttner P, Stadler R, Guggenmoos-

Holzmann I, Orfanos CE. Epidemiologic evidence for the

role of melanocytic nevi as risk markers and direct precursors

of cutaneous malignant melanoma. Results of a case control

study in melanoma patients and nonmelanoma control

subjects. J Am Acad Dermatol. 1992 Jun;26(6):920-6. doi:

1016/0190-9622(92)70133-z. PMID: 1607409.

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Published

2026-09-02

How to Cite

1.
Sharma R, Khamankar S, Bhat D. Histopathological spectrum of Pigmented Melanocytic Lesions . IJPBR [Internet]. 2026Sep.2 [cited 2026Sep.14];14(03):390-4. Available from: https://ijpbr.in/index.php/IJPBR/article/view/1363