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Identifying the clinical and histopathological characteristics of amelanotic melanoma: a case series

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Identifying the clinical and histopathological characteristics of amelanotic melanoma: a case series. / Sohail, Aroon; Kavaklieva, Svetlana.
In: Oxford Medical Case Reports, Vol. 2024, No. 4, omae029, 25.04.2024.

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Sohail A, Kavaklieva S. Identifying the clinical and histopathological characteristics of amelanotic melanoma: a case series. Oxford Medical Case Reports. 2024 Apr 25;2024(4):omae029. doi: 10.1093/omcr/omae029

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Sohail, Aroon ; Kavaklieva, Svetlana. / Identifying the clinical and histopathological characteristics of amelanotic melanoma : a case series. In: Oxford Medical Case Reports. 2024 ; Vol. 2024, No. 4.

Bibtex

@article{87553d0e783449859ac2fca19b3d36b4,
title = "Identifying the clinical and histopathological characteristics of amelanotic melanoma: a case series",
abstract = "Amelanotic melanoma (AM) is a subtype of melanoma where the lesion demonstrates no pigmentation. This can lead to delays in referral with studies showing a higher mortality rate. To determine the characteristics of AM lesions, we conducted a retrospective analysis of patients with confirmed AM. Of the 16 patients, 68.75% were male and the mean age at diagnosis was 78 years. The most common location for AM was the head (37.5%) which also demonstrated a higher mitotic rate (10.67 mm2) compared to the average (7.31 mm2). More than half of the lesions (56%) had been present for more than 1 year. With a misdiagnosis rate of 87.5%, the likelihood of delays were evident. There was no unifying feature on clinical assessment, however conspicuous vessel findings were noted on 62.5% of lesions. We have demonstrated that AM continues to remain a missed diagnosis with the potential for a more lethal cancer to form.",
author = "Aroon Sohail and Svetlana Kavaklieva",
year = "2024",
month = apr,
day = "25",
doi = "10.1093/omcr/omae029",
language = "English",
volume = "2024",
journal = "Oxford Medical Case Reports",
issn = "2053-8855",
publisher = "Oxford University Press (OUP)",
number = "4",

}

RIS

TY - JOUR

T1 - Identifying the clinical and histopathological characteristics of amelanotic melanoma

T2 - a case series

AU - Sohail, Aroon

AU - Kavaklieva, Svetlana

PY - 2024/4/25

Y1 - 2024/4/25

N2 - Amelanotic melanoma (AM) is a subtype of melanoma where the lesion demonstrates no pigmentation. This can lead to delays in referral with studies showing a higher mortality rate. To determine the characteristics of AM lesions, we conducted a retrospective analysis of patients with confirmed AM. Of the 16 patients, 68.75% were male and the mean age at diagnosis was 78 years. The most common location for AM was the head (37.5%) which also demonstrated a higher mitotic rate (10.67 mm2) compared to the average (7.31 mm2). More than half of the lesions (56%) had been present for more than 1 year. With a misdiagnosis rate of 87.5%, the likelihood of delays were evident. There was no unifying feature on clinical assessment, however conspicuous vessel findings were noted on 62.5% of lesions. We have demonstrated that AM continues to remain a missed diagnosis with the potential for a more lethal cancer to form.

AB - Amelanotic melanoma (AM) is a subtype of melanoma where the lesion demonstrates no pigmentation. This can lead to delays in referral with studies showing a higher mortality rate. To determine the characteristics of AM lesions, we conducted a retrospective analysis of patients with confirmed AM. Of the 16 patients, 68.75% were male and the mean age at diagnosis was 78 years. The most common location for AM was the head (37.5%) which also demonstrated a higher mitotic rate (10.67 mm2) compared to the average (7.31 mm2). More than half of the lesions (56%) had been present for more than 1 year. With a misdiagnosis rate of 87.5%, the likelihood of delays were evident. There was no unifying feature on clinical assessment, however conspicuous vessel findings were noted on 62.5% of lesions. We have demonstrated that AM continues to remain a missed diagnosis with the potential for a more lethal cancer to form.

U2 - 10.1093/omcr/omae029

DO - 10.1093/omcr/omae029

M3 - Journal article

VL - 2024

JO - Oxford Medical Case Reports

JF - Oxford Medical Case Reports

SN - 2053-8855

IS - 4

M1 - omae029

ER -