Solitary cutaneous neoplasms: analysing the uncertain behaviour with the aid of histopathology

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Abstract

BACKGROUND: Skin tumours can be classified as either benign or malignant, resulting due to the proliferation of one or more components of the skin. Reportedly, there has been a rise in the prevalence of skin cancer in recent decades, which has led to rely on histological evidence to distinguish between various types of skin cancer.

AIM: This study aims to provide a comprehensive description of the occurrence, symptoms, unpredictable nature, and range of histopathological spectrum in different types of skin tumours.

METHODS: This prospective research was conducted in the outpatient department of the Department of Dermatology at the Government General Hospital in Anantapur from July 2019 to July 2023. Patients who did not provide informed consent, those with infectious or cystic swellings, or those with multiple lesions were excluded from this study. Histopathological confirmation is obtained from all excisional biopsies of single cutaneous swellings, and tumours are classified based on the criteria established by the World Health Organization (WHO).

RESULTS: The study included a total of 123 individual cutaneous tumours, with 98 cases (79.67%) being classified as benign and 25 cases (20.32%) classified as malignant. The age group most affected is adults between the ages of 26 and 44, with a prevalence rate of 31.7%. Following closely behind are middle-aged individuals, with a prevalence rate of 30.08%. The males constitute 46.34% (57 cases) and the females constitutes 53.65% (66 cases). The extremities were the most frequently affected site, accounting for 53 cases (43.08%), followed by the head and neck region (29.26%). Based on the WHO classification of skin tumours, there were 42 cases (34.14%) of subcutaneous tissue tumours and 31 cases (25.20%) of soft tissue tumours. The prevalence of keratinocyte tumours is 26 (21.13%), whereas appendageal tumours account for 16 (13%) of cases. Melanocytic and neural tumours are the least prevalent, each representing 4 (3.25%) of cases. The majority of benign tumours arise from the subcutaneous tissues, whereas malignant tumours grow from keratinocytic differentiation.

CONCLUSION: Our study revealed that the majority of tumours displayed ambiguous clinical behaviour, which resulted in erroneous diagnoses. Hence confirmation by histopathology is crucial for accurate diagnosis and prompt management.

About the authors

Lekkala Sreedevi

Government Medical College

Author for correspondence.
Email: drsreelekkala@gmail.com
ORCID iD: 0009-0006-3239-320X

Associate Professor of DVL

India, Anantapur, Andhra Pradesh

D. Edukondala Rao

Andhra Medical College

Email: dhanyasiekora39@gmail.com
ORCID iD: 0009-0002-2440-8994

Associate Professor of DVL

India, Visakhapatnam, Andhra Pradesh

A. Vijaya Kumari

Government Medical College

Email: drvijayakabburam@gmail.com

Associate Professor of DVL

India, Anantapur, Andhra Pradesh

Machani Niharika

Government Medical College

Email: harikamachani@gmail.com
ORCID iD: 0009-0009-7709-8302

Junior Resident of DVL

India, Anantapur, Andhra Pradesh

P. Sravani

Government Medical College

Email: chenna2593@gmail.com
ORCID iD: 0000-0001-8859-6758

Associate Professor of Pathology

India, Anantapur, Andhra Pradesh

V. Sivasankara Naik

Government Medical College

Email: vssnaik73@gmail.com
ORCID iD: 0009-0001-5792-5456

Professor & HOD of Pathology

India, Anantapur, Andhra Pradesh

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Supplementary files

Supplementary Files
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1. JATS XML
2. Fig. 1. Bar diagram showing number of patients based on tumour origin according to WHO classification.

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3. Fig. 2. Pyogenic granuloma: (a) reddish pink small nodule over right side of lower neck (b) nodular proliferation of blood vessels with RBC (H &E ×400).

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4. Fig. 3. Nevus sebaceous: (a) hyperpigmented plaque with verrucous surface noted over scalp with few hairs (b) epidermal papillomatosis, arrow denotes mature sebaceous lobules, no hair shaft (H &E ×400).

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5. Fig. 4. Keratoacanthoma: (a) flesh coloured dome shaped nodule with central keratin crater (b) keratin filled crater (c) dyskeratotic cells are conspicuous (H &E ×400).

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6. Fig. 5. Pie chart showing percentage of Benign tumours, %.

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7. Fig. 6. Melanoacanthoma: (a) hyperpigmented hyperkeratotic plaque over right side of back mimicking melanoma (b) Tumour cells arranged in papillae with central melanin deposition and extracellular melanin (H &E ×400).

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8. Fig. 7. Pilomatricoma: (a) hemispherical hard nodular swelling noted over right forearm mimicking calcinosis cutis (b) green arrows denotes characteristic ghost cells (H &E ×400).

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9. Fig. 8. Dermatofibroma: (a) hyperpigmented firm to hard nodule over left hand mimicking calcinosis cutis (b) red arrows denotes numerous elongated spindle cells proliferation (H &E ×400).

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10. Fig. 9. Squamous cell carcinoma — verrucous type: (a) solitary ill-defined flesh coloured verrucous plaque with crusting (b) HPE image showing papillary growth denoted by red arrows, dysplastic epithelium denoted by red asterisk and keratin pearls denoted by red square (H &E ×400).

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11. Fig. 10. Basal cell carcinoma: (a) black coloured irregular shaped plaque below the right eye (b) palisading of atypical basaloid cells separated by fibrous stroma denoted by black arrow and have retraction artifacts denoted by black circle (H &E ×400).

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12. Fig. 11. Malignant melanoma: (a) hyperpigmented hyperkeratotic plaque over left sole (b) infiltration of tumour cells into dermis denoted by red asterisk (c) prominent eosinophilic nucleoli denoted by red arrows (H &E ×400).

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13. Fig. 12. Bowens disease: (a) brownish black plaque with rough surface noted over left thigh mimicking lupus vulgaris (b) hyperplastic epidermis with severe dysplasia but not infiltrating dermis denoted by red asterisk (c) (H &E ×400).

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14. Fig. 13. Proliferating trichilemmal tumour: (a) smooth surfaced swelling over right frontal side of scalp mimicking sebaceous cyst (b) Proliferating lobular growth (c) severe keratinocytic nuclear atypia with cSCC transformation (H &E ×400).

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15. Fig. 14. Pie chart showing percentage of malignant tumours, %.

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