Please login or create an account. If you do not have access to this content, you will be shown a 30 second preview and licensing options.
- Presentation
Melanoma in Pregnancy: Dispelling Myths and Reviewing Diagnosis, Prognosis, and Treatment
Description
The talk dispels common myths about melanoma in pregnancy, arguing that pregnancy does not generally worsen melanoma prognosis and that many alarming claims are based on flawed or misinterpreted studies. It reviews evidence that melanocytic nevi usually do not undergo true physiologic atypia during pregnancy; while some lesions, especially on the abdomen and breasts, may show mild enlargement or vascular changes, any clinically, dermoscopically, or histologically atypical lesion should still be biopsied rather than assumed benign. Women with dysplastic nevi or a personal/family history of melanoma should be monitored more closely, often each trimester. For melanoma itself, large controlled studies generally show no difference in survival, recurrence, or tumor features between pregnant and non-pregnant patients, and prior or subsequent pregnancies usually do not worsen outcomes. The lecture emphasizes timely diagnosis, notes that melanoma is the cancer most likely to metastasize to the placenta and fetus, and recommends placental histologic examination when melanoma occurs in pregnancy. Treatment guidance includes standard excision, careful use of anesthesia, selective use of sentinel node biopsy, and appropriate imaging with pregnancy precautions; stage I/II treatment is similar to non-pregnant patients, while newer targeted therapies are teratogenic and should be avoided during pregnancy and breastfeeding. The speaker also concludes that oral contraceptives and hormone replacement therapy have little to no meaningful impact on melanoma risk in most settings.
View moreConclusions
- Melanoma during pregnancy generally behaves like melanoma in non-pregnant patients, with no consistent evidence of worse survival or recurrence from pregnancy itself.
- Most changes seen in ordinary melanocytic nevi during pregnancy are not evidence of malignancy, and any clinically, dermoscopically, or histologically atypical lesion should be biopsied rather than assumed to be physiologic.
- Women with dysplastic nevi or a personal/family history of melanoma warrant closer surveillance during pregnancy, typically with photography and trimester-based follow-up.
- The apparent association between pregnancy and worse melanoma outcomes in some reports is likely explained largely by delayed diagnosis and methodological flaws rather than a true biologic effect of pregnancy.
- Pregnancy-associated melanoma is not a reason to automatically defer future pregnancies after a thin or localized melanoma, though higher-risk cases may justify an individualized delay.
- When melanoma is diagnosed during pregnancy, standard management principles still apply, with surgery, imaging, and sentinel node evaluation possible using pregnancy-adapted precautions.
- Advanced melanoma in pregnancy requires special attention to placental examination because melanoma is the cancer most likely to metastasize to the placenta and, rarely, the fetus.
- Early-stage melanoma has little to no demonstrated adverse effect on fetal or gestational outcomes, whereas widespread maternal disease can drive neonatal risk.
- Oral contraceptives and hormone replacement therapy do not show a strong, consistent melanoma risk signal in most studies, so routine withholding is generally not supported by the evidence.
- Tellez, Rueda, Conic, Galdyn, Mesinkovska, Gastman. Risk factors & outcomes of cut melanoma in women less than 50 years of age. JAAD 2016;74(4):731-738.#10.1016/j.jaad.2015.11.014
- Carter TJ, et al. Melanoma in pregnancy Dx & management in early stage & advanced disease. Eur J Cancer 2022;166:240-253.#10.1016/j.ejca.2022.02.016
- Chan, et al. J Cutan Pathol 2010;37:843.
- Pennoyer, Grin, Driscoll, Dry, Walsh, Gelineau, Grant-Kels. JAAD 1997;36:378.
- Martins-Costa GM, Bakos R. Dermatol Pract Concept 2019;30;9(2):126-131.
- Ellis DL. JAAD 1991;25:467.
- Borges, et al. Actas Dermosifiliogr 2011;102:650.
- O’Meara et al. 2005.
- Lens et al. 2004.
- Davidson TM, et al. Pregnancy-associated melanoma: characteristics & outcomes from 2002 to 2020. Melanoma Res. 2024;34(2):175-181.#10.1097/cmr.0000000000000953
- Byrom, et al. Increased mortality for pregnancy-associated melanoma. J Eur Acad Dermatol Venereol 2015;29:1457-66.
- Kiuru M, et al. JEADV 2022;36(11):2025-2035.
- Slinguff et al. Ann Surg 1990;211:552.
- MacKie et al. Lancet 1991;337:653.
- Travers, et al. Br J Derm 1995;132:876.
- de Giorgi V, et al. Arch Dermatol 2009;145:30.
- Bannister-Tyrrell, et al. Aust NZJ Obstet Gynaecol 2015;55:116.
- Merkel, et al. JAAD 2016;74:88-93.
- Baergen et al. 1997.
- Alexander et al. 2003.
- Altman et al. 2003.
- Amer College of Ob & Gyn's Committee on Ob Practice, Committee Opinion No. 656 Guidelines for Diagnostic Imaging During Pregnancy & Lactation. Obstet Gynecol 2016;127:e75.#10.1097/00006250-201602000-00055
- Heggarty E, et al. JAAD 2025;93(5):1337-1339.
- Gupta and Driscoll, Clinical Dermatology.
- Karagas et al. British Journal of Cancer.
- Donley et al. British Journal of Dermatology.
- Cervenka et al.
- Olsen et al.