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Acral Lentiginous Melanoma
Introduction
Acral lentiginous melanoma (ALM), also sometimes referred to as, simply, acral melanoma, is melanoma occurring on the hands and feet (palms, soles, fingers, toes, and nail units). The word acral derives from the Greek word referring to the highest or topmost portion of the limbs (extremities). The same stem word is used for the city of Akron (in Summit County, Ohio, the highest elevation on the Ohio and Erie Canal), and the acropolis (the rocky outcrop in Greece on which the Parthenon sits). Lentiginous refers to the initial origin of these tumors as a macular (flat) brown spot, resembling a benign lentigo.
The term melanoma refers to a malignancy of melanocytes, the pigment-producing cells in the epidermis. Acral melanoma was first separated as a distinct subtype of cutaneous malignant melanoma (CMM) by Arrington et al. in 1977.[1] It is the least common subtype of melanoma, comprising only 2 to 3% of total melanoma diagnoses. Unlike other CMM, UV-radiation is not thought to play a significant part in the development of ALM. It is most commonly on the lower extremities and is often advanced at the time of presentation leading to a high level of morbidity and mortality.[2][3][4] It has a higher proportional incidence in non-white populations compared to other subtypes of melanoma.[2] In this article, we will discuss the unique aspects of this disease.
Etiology
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Etiology
Multiple studies proposed stress, or shearing force as a mechanism for the induction of ALMs, as the incidence is higher in the weight-bearing areas of the foot, such as the heel, forefoot, and lateral side of the foot.[5][6][7] Melanoma in the arch is rarer, however, was found to occur more frequently in obese patients.[8] However, most recently, Ghanavatian et al. found that once corrected for surface area, ALM was inversely proportional to atypical acral nevi and benign acral nevi in weight-bearing areas of the foot.[9] ALM may have an increased incidence on plantar surfaces compared to the palm, due to 50% more melanocytic density on the sole.[10] There has been some correlation in the literature with penetrative injuries increasing the likelihood of ALM compared to control patients without penetrative injury.[11][12] Typical mutations identified in other types of CMM, which are UV-induced, are not identified in ALM. The pathogenesis of ALM remains unclear, but genetic factors have been found to contribute.
Epidemiology
ALM accounts for 2 to 3% of all new melanomas. The average age of diagnosis for ALM is 62.8 years. The incidence of ALM in all populations increases with age, and a sharp increase is seen in incidence per person year after the age of 80. Similar numbers of males and females are affected; however, females are more commonly diagnosed at an earlier stage than males. ALM has a disproportionately higher incidence in non-white patients compared to other melanoma subtypes.[3] It does not represent the most common type of melanoma in any racial group in United States-based studies.[4]
Although studies from Mexico, Taiwan, and China have found it to be the most common subtype in their populations.[13][14][15] In two United States population-based registry studies, Bradford et al. and Huang et al. found that ALM accounted for 33-36% of CMM in Blacks. ALM represented 18-23.1% of total CMM in Asian/Pacific Islanders. ALM represented 9% of CMM diagnosed in Hispanic Whites and only 1% in non-Hispanic Whites.[3] Incidence rates of ALM were highest in Hispanic Whites at 2.5 per 1,000,000 person-years and significantly lower in Blacks, Non-Hispanic Whites, and Asian/Pacific Islanders at 1.8, 1.8, and 1.1 per 1,000,000 person-years, respectively.[2] Melanoma specific survival (MSS) was lower in Black and Hispanic White populations at 5 and 10 years than whites; however, when controlled for Breslow depth, no difference was seen. This is thought to be attributable to the advanced stage at presentation in these minority groups.[3]
Pathophysiology
ALM, like mucosal melanomas, is a low mutational burden sub-type of melanoma and does not carry UV-radiation induced mutations that are commonly seen in other CMMs.[16][17][18] Common gene mutations in ALM include KIT, BRAF, NRAS, and NF1.[16][19] Specifically, KIT copy number gains are seen in up to 36% of acral melanomas, which is thought to be the most common mutation in ALM, which is much higher than other CMM. In one study, the most commonly identified molecular aberration was chromosomal instability in the Cyclin D1 gene and was seen in 45% of ALM. Cytologically typical melanocytes which surround the atypical lesion often harbor KIT copy number gains and Cyclin D1 mutations, which is a concept known as 'field effect' and may explain local recurrences after excision of the clinical lesion.
In a paper on FISH analysis of ALM, CCND1 gains, MYC gains, and CDKN2A loss were common alterations seen in their cohort. TERT promoter mutations, commonly found in UV-radiation induced melanomas, are not prevalent in ALM; however, other mutations involving the TERT gene including copy gains, translocations, missense, and promoter mutations were found in up to 41% of cases.[16] It has been proposed by Su, J. et al. that the carcinogenesis of ALM could be ethnicity dependent, which might help explain the large variety of genetic aberrations seen in the literature.[20][21]
Histopathology
ALM is characterized by a broad radial growth phase in which the melanocytic neoplasm remains in-situ. In this phase, single atypical melanocytes are increased predominately at the dermo-epidermal junction in a lentiginous pattern with a propensity to involve the adnexal structures.[22] In an advanced in-situ lesion, rare nests can be seen, and they are typically larger, more discohesive, and variable in size and shape compared to their benign counterparts.[4] Pagetoid spread, a common feature of both benign and malignant acral melanocytic lesions can be prominent at the peripheral edges and within the ridges, which impart the characteristic dermoscopic findings of “parallel ridges” that is associated with acral melanocytic malignancy.[4][23] Cytologic atypia of melanocytes can be prominent in ALM and manifests as nuclear hyperchromasia, increased size, and variable shape. Invasion occurs typically many years after the lesion begins and consists of nested or single melanocytes invading the dermis. The invasive portion of ALM lesions typically resembles superficial spreading melanoma but may progress to a more nodular morphology with time.
Histopathologic evaluation of acral melanocytic lesions is difficult as the lesions may be subtle and heterogenous microscopically.[24] This is further complicated by the partial sampling of lesions due to the large lesion size at presentation.[25] Additionally, because of the unique diagnostic features of acral melanocytic lesions, special attention must be paid when gross dissection is performed to ensure sectioning perpendicular to the dermatoglyphics and is best accomplished by experienced laboratory personnel.
History and Physical
ALM is most commonly an acquired lesion and is associated with a previously existing nevus in less than 11% of cases.[26] It typically begins as a macule progressing to a patch with variable light to dark brown pigment. The edges are typically angular, often following the ridges of the dermatoglyphics. As the lesion progresses and invades, it may become nodular and darkly pigmented, appearing blue to black. Ulceration may occur as the lesion becomes more nodular.
It has been proposed the that classical “ABCDE” approach for melanoma be replaced on acral surfaces with the “CUBED” acronym which stands for colored lesions where any part is a different color, uncertain diagnosis or a lesion without a clear clinical diagnosis, bleeding lesions, enlargement of a lesion, and a delay in healing beyond two months.[27]
The dermoscopic examination is a useful adjunct for pigmented acral lesions to help identify worrisome pigment patterns.[28] Two systems to assess pigmented acral lesions on dermoscopy have been proposed. The first by Koga and Saida is a 3-step algorithm. Concerning features of an acral lesion on dermoscopy, include a parallel ridge pattern and/or lack of typical features of an acral nevus (i.e., fibrillar, lattice-like, and parallel furrow patterns) and a size greater than 7 mm.[29] The second, by Lallas et al., uses six dermatoscopic variables to assess the likelihood of ALM under the acronym BRAFF.[30] Four positive variables include blotches, ridge pattern, asymmetry of structures, and colors, and two negative variables include furrow pattern and fibrillar pattern. Despite the dermoscopic and clinical appearance, lesions greater than 7 mm in diameter should be biopsied, and all lesions greater than 9 mm are likely to be melanoma.[28][31]
ALM of the nail unit will often present as diffuse pigmentation of the nail, pigmented striping of the nail, or other non-pigmented changes, such as ulceration. The thumb and great toe are the site of subungual ALM in 92% of cases.[10] When pigment from a subungual ALM extends into the nail fold, it is known as Hutchinson sign and is a worrisome clinical feature. The lesion may begin as a subungual ALM with pigment isolated to the nail fold; however, extension into the adjacent glabrous skin is common with advanced lesions.
Evaluation
For clinically suspected melanomas, narrow margin excisional biopsy is recommended; however, it is acknowledged in the recommendations that this may be impractical on an acral site.[32] A partial sampling of the lesion is then considered an acceptable alternative, although the main risk with partial sampling is that it may result in an inaccurate histologic diagnosis. The most nodular portion of the lesion should be sampled so that an accurate Breslow depth can be determined. With suspicious nail lesions, nail matrix sampling is necessary. The surgical techniques in nail sampling are complicated and should be referred to a provider skilled in these techniques to ensure diagnostic accuracy.[32] Subsequently, biopsy evaluation by a dermatopathologist is often required as the findings in ALM may be subtle and require a high level of clinicopathologic correlation.
If the patient is shown to have the local cutaneous disease and is otherwise asymptomatic, imaging studies and other laboratory tests such as blood work are not recommended.[32] In later stage disease, lactate dehydrogenase levels, while not usually the sole indicator of metastatic disease, are a good predictor of survival in patients with stage IV disease.[33]
Radiologic assessment to detect occult nodal disease or distant metastases has a high rate of false positives. However, if imaging is obtained, a chest x-ray should be considered as a cost-effective option. Gratuitous imaging may result in unnecessary invasive procedures. The American Academy of Dermatology suggests yearly skin exam and regional lymph node palpation as sufficient to assess for recurrence.[32]
Sentinel lymph node biopsies have high prognostic value in intermediate and thick melanomas. In patients with intermediate thickness melanomas and sentinel lymph node metastases, the melanoma-specific survival (MSS) was 62.1% when sentinel lymph node biopsy and completion lymphadenectomy were performed, but only 41.5% in the observation group who had a completion lymphadenectomy after clinical nodal metastases were identified.[34] The MSS was not affected significantly in patients with thick melanomas who underwent sentinel lymph node biopsy. Despite the previously mentioned study, these findings do remain controversial, with many authors questioning the survival benefit of sentinel lymph node biopsies.[32]
Treatment / Management
Wide local excisions are the mainstay for ALM. Definitive surgical margin recommendations are based on tumor thickness at the time of biopsy, which is further discussed in the surgical oncology section. Foregoing surgical excision of in-situ lesions when surgery is not practical can be considered.
Off label use of topical imiquimod has been studied; however, the persistence of in-situ lesions, failure to detect invasive lesions due to lack of excision, the progression of lesions, and the high cost of treatment are all potential pitfalls of this treatment. If metastases are detected clinically, by palpation of local lymph node beds, or by sentinel lymph node biopsy, systemic treatment with chemotherapeutic agents, targeted mutational therapy, and immune checkpoint inhibitors may be indicated which is further discussed below in the oncology section. Patients who have asymptomatic high stage disease do not show a survival benefit from treatment before symptoms arise.[32]
Differential Diagnosis
The differential diagnosis for ALM is relatively broad. The differential includes other melanocytic neoplasms such as lentigo, congenital acral nevi, and acquired acral nevi. The differential for subungual ALM includes ethnic pigmentation, lentigo, and nevi. Other non-melanocytic lesions that may mimic ALM on the glabrous skin and subungual nail include fungal and bacterial infections, trauma-related hemorrhage (talon noir), terra firma-forme dermatosis, chronic wounds, verrucae, and other skin cancers which may be secondarily pigmented such as squamous cell carcinoma or porocarcinoma.[35][36]
Surgical Oncology
Wide local excision is the primary treatment for ALM.
The suggested excision depth is to the fascia or deep adipose, depending on the location. The AAD and AJCC guidelines suggest variable clinical, surgical margins depending on Breslow depth[32]:
- In-situ lesions: 0.5 to 1 cm clinical margins
- Breslow depth less than 1 mm: 1 cm clinical margin
- Breslow depth between 1.01 to 2 mm: 1 to 2 cm clinical margin
- Breslow depth greater than 2 mm: 2 cm clinical margin
Large defects on acral surfaces are hard to close primarily and may require skin grafting or flap reconstruction. Primary closure has better functional results, heals faster, leads to fewer patient complications, and has a lower cost.[37] Healing by secondary intention is an acceptable alternative. With tissue defects larger than 1.5 cm, an alternative form of closure will help prevent painful scars and contractures.[38] For ALM located on the digits, wide local excisions have been shown to have a similar prognosis compared to amputations.[39]
Subungual melanomas are difficult to resect due to the proximity to the phalanx. The previous gold standard of treatment involved digit amputation.[40] More recently, a review of 67 cases of conservative surgical excision of subungual melanoma determined wide local excision without removal of bone, followed by full-thickness skin graft had better functional outcomes for the patient with good cosmesis and achieved the same disease-free survival interval.[41] A prospective multi-institutional trial is currently underway with the goal to confirm that conservative non-amputation treatment of subungual melanoma is a safe and efficacious treatment.[40]
Radiation Oncology
Radiation therapy is not commonly viewed as a primary approach to treating these lesions since melanocytes are not highly radiosensitive. However, this treatment has been used for adjuvant treatment, palliation, and for patients with recurrent disease.[42]
Medical Oncology
Dacarbazine had been the mainstay of metastatic melanoma chemotherapy, until the recent advent of immune checkpoint inhibitors and mutation-driven therapy; however, it never showed a clear survival benefit.[43][44]
Metastatic ALM has been shown to be less susceptible to immune checkpoint inhibitors owing to a poor immune response to the tumor.[43] PDL1 was found to be expressed in 31% of ALMS with a lower number of tumor-infiltrating lymphocytes (TILs) than other types of melanoma.[45] Immune stimulators such as imiquimod, dacarbazine, and interferon may help increase TILs within ALM and thus increase the ability of the immune checkpoint inhibitors to function.[43] Imiquimod on its own has been shown to prevent progression and even regression of ALM.[46][47] However, utility in acral skin with thick stratum corneum may be limited.[43]
While other types of CMM harbor frequent BRAF mutations, ALM rarely has these mutations and is thus less susceptible to the commonly used BRAF/MEK inhibitors. NRAS mutations may cause the resultant tumor to be susceptible to BRAF and MEK inhibitors due to the location of the NRAS upstream of BRAF.[43] Increased KIT mutations seen in ALM can be targeted with KIT inhibitors. However, studies have shown imatinib, KIT inhibitor, to be more successful in treating CMM with KIT mutations than with KIT copy number gains, as seen in ALM.[48]
Staging
Staging for all subtypes of melanoma is the same and based on the American Joint Committee on Cancer (AJCC) Cancer Staging Manual, 8th Edition.[49] There are four stages, 1 to 4, which are based on various parameters of the TNM pathologic grading system. Below is a brief summary.
- Stage 1: T1a, T1b, T2a primary lesions with no nodal, regional, or distant metastases
- Stage 2: T2b, T3a, T3b, T4a, T4b primary lesions with no nodal, regional, or distant metastases
- Stage 3: Any primary lesion with regional nodal or in-transit metastases
- Stage 4: Any primary lesion with distant metastases.
Prognosis
Prognosis in ALM depends on the evaluation of multiple clinicopathologic factors. Disease-specific survival is affected by gender, race, age, Breslow thickness, ulceration, pathologic stage, and sentinel lymph node positivity.[3] In two studies, through multivariant analysis, positive sentinel lymph nodes were the strongest predictor of disease recurrence and death from melanoma.[34][15] Compared to CMM at the same stage and depth, ALM has lower respective survival rates [3][50][51][50][52] with few studies finding that survival rates are similar.[53]. ALMs often present at a more advanced stage, which is thought to be multifactorial in cause. Contributing to this is difficulty in observation of the soles of the feet by the elderly, lack of knowledge in minority populations about their risk for melanoma, decreased access to care, and other cultural factors.
Complications
Large excisions of ALM, particularly on the hands, can lead to contractures and painful scarring, which can lead to significant morbidity.[38] If digit or limb amputation is required for treatment, patients can experience significant interference with activities of daily living, loss of function of the affected limb, phantom pain, and poor cosmetic outcomes.[40]
Deterrence and Patient Education
Because the causation of ALM cannot be attributed to any specific exposure, avoidance is difficult. Patient education and early detection make the most difference in disease-specific survival. Increased education is necessary for populations who have a low incidence of sun-induced melanoma as they have decreased MSS compared to non-Hispanic White populations and may be less aware of the warning signs of melanoma.[53]
Pearls and Other Issues
1. Benign acral nevi are more likely to have pigment found in the furrows of the dermatoglyphic lines, as opposed to acral melanomas, which are more likely to have pigment accentuated in the elevated ridges. There is an adage saying "furrows are fine, ridges are risky," referring to the pigment accentuation viewed with magnification or dermoscopy.
2. Dirt on the soles (terra firma-forme dermatosis) can resemble acral nevi, but usually will rub off with an alcohol prep.
3. Tinea nigra, a pigmented fungus found in warm climates, has been mistaken for melanoma, and unnecessary surgeries have been performed on these lesions. A simple KOH-preparation will reveal the hyphae.
4. Talon noir (French for black heel) can resemble acral melanoma. This is simply blood in the stratum corneum from trauma, common from running or other activity. Examination with dermoscopy can often eliminate the need for biopsy.
5. Small incomplete biopsies can be misinterpreted as benign by the pathologist. It is best to sample the entire lesion, when possible. If the lesion is large, then alert the pathologist of the total lesion size on the requisition, to increase suspicion.
6. Shave biopsies are difficult to perform on thick acral skin and often result in samples that are too superficial. Usually, a punch biopsy or excisional biopsy is better.
7. Benign acral nevi can have pagetoid melanocytes (cells that ascend upward through the epidermis as do adenocarcinoma cells in Paget's disease) in one-third of cases, causing a misdiagnosis of acral melanoma. In benign acral nevi, the pagetoid cells are more likely to be limited to the central portion of the lesion, whereas in melanomas, the pagetoid cells are more likely to extend into the margins. Acral nevi have been called MANIAC nevi (melanocytic acral nevus with the intraepidermal ascent of melanocytes).
Enhancing Healthcare Team Outcomes
An interprofessional approach is paramount in providing care for patients with ALM. Primary care providers play an important role in patient education and the detection of early changing skin lesions. Once detected, dermatologists are often consulted to confirm the suspicious nature of the lesion and perform the initial biopsies. Evaluation of the lesional biopsy by a trained dermatopathologist is also necessary as the diagnosis is difficult and requires significant clinicopathologic correlation. Treatment may involve multiple specialties include Mohs surgeons, general surgeons, or orthopedic surgeons for definitive excision of the lesion. If metastases are expected, surgical oncology and hematology/oncology should be consulted to facilitate sentinel lymph node biopsy and consider systemic therapies as warranted.
Media
(Click Image to Enlarge)
Asymmetric Parallel Ridge Dermoscopic Pattern Indicative of Acral Lentiginous Melanoma on the Heel of a 62-Year-Old Male.
Contributed by M Bodman, DPM
(Click Image to Enlarge)
Clinical Photo of an Ulcerated Acral Lentiginous Melanoma on the Dorsal Aspect of a Toe.
Contributed by RP Rapini, MD
(Click Image to Enlarge)
Clinical photo of an acral lentiginous melanoma. This large lesion has irregular borders and has variable pigmentation from light brown to black. Contributed by Ronald Rapini, MD.
(Click Image to Enlarge)
This Hematoxylin and Eosin stained section of an acral lentiginous melanoma in-situ shows large atypical melanocytes with pleomorphic and hyperchromatic nuclei arranged along the dermal-epidermal junction. Contributed by Ronald Rapini, MD.
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