INTRODUCTION
Marjolin’s ulcer (MU), also called cicatricial carcinoma, is a lesion first described
in 1928 by the French surgeon Jean Nicholas Marjolin after observing tumor lesions
originating from burn scars. The incidence ranges from 0.77 to 2%1,2. As for the time of progression, it is considered a chronic form when the time of
evolution of the lesion is greater than 12 months. The average time of malignant transformation
is generally superior to 30 years3,4,5. Although the evolution, in most cases, is slow, early diagnosis is essential since,
in the initial stages, the malignant tumor is subject to excision with less complex
reconstructions6.
The diagnosis of Marjolin’s ulcer is made through the patient’s clinical history,
lesion presentation, and histopathology. Although a previous history of burns is the
most frequent cause, other factors such as pressure ulcers, ulcers due to dermatological
conditions, lesions due to vascular insufficiency, and ulcers due to diabetes, among
others, are indicative predictors3.
Histopathologically, it can be classified into squamous cell carcinoma (SCC), the
latter developed in white populations, especially after exposure to ultraviolet rays,
basal cell carcinoma (BCC), melanoma, sarcoma, and other rare cell types7. It has a wide spectrum of differential diagnoses, such as ulcerative infectious
diseases such as tertiary-stage syphilis, American tegumentary leishmaniasis, sporotrichosis,
and leprosy.
Marjolin’s ulcer treatment is a process that requires knowledge and preparation. The
most specific treatment is surgery, radiotherapy is recommended in particular cases,
and chemotherapy has shown little efficacy1,8.
OBJECTIVE
The purpose of this study is to review this condition, highlighting the history, physical
examination, local care, clinical and surgical treatment, and its impact on prognosis
and quality of life.
METHOD
This is a literature review based on original studies and trials published between
2005 and 2020 in English and Portuguese, with or without systematization. The search
was carried out in the Medline and SciELO databases, using the descriptors “Squamous
Cell Carcinoma,”; “Marjolin’s Ulcer,”; “Postburn Wounds.” Nine articles were selected,
of which 8 refer to the Medline database and 1 to the SciELO database, because they
fit the requirements and are relevant to the analysis and discussion. Furthermore,
data released by the Brazilian Society of Dermatology, the Revista Brasileira de Cirurgia Plástica, the Ministry of Health, and protocols and guidelines were consulted to enrich the
discussion of this article.
RESULTS
In total, 382 published scientific articles addressing the issue of Marjolin’s ulcer
were found. After reading the abstracts and information in each study, we selected
21 articles to compose and support our bibliographic review. Of these 21, 9 articles
meet the requirements of being observational, analytical, or descriptive studies,
then analyzed and presented in our table of results (Chart 1).
Chart 1 - Observational studies on Marjolin’s ulcer (UM).
Authors |
Title |
Year |
Results |
Type of Study |
Xiang et al.1 |
Clinical features and treatment of 140 cases of Marjolin's ulcer at a major burn center
in southwest China
|
2019 |
MU occurred mainly in men and resulted from scar carcinoma after burns. The pathological
type was mainly squamous cell carcinoma. Autologous skin grafting and local skin flap
repair were the main repair methods used. The skull bone was the site most susceptible
to invasion.
|
Retrospective Study |
Bang & Woo2 |
The Fate of Chronic Burn Wounds Suspected as Marjolin's Ulcers |
2018 |
Histologically, chronic ulcer and pseudoepitheliomatous hyperplasia were 21%, respectively,
and malignancy, including squamous cell carcinoma and leiomyosarcoma, was 58%. The
mean latency period was 31.6±13.0 years, and most injuries occurred in the extremities.
|
Retrospective Study |
Kerr-Valentic et al.3 |
Marjolin's Ulcer: modern analysis of an ancient problem |
2009 |
Although burn scarring represents 76.5% of patients in the authors' review, venous
stasis ulcers, traumatic wounds, osteomyelitis, and pressure ulcers are also types
of wounds that can undergo malignant degeneration.
|
Cross-sectional study with bibliographic review |
Choi et al.4 |
Impact of Disturbed Wound Healing after Surgery on the Prognosis of Marjolin's Ulcer |
2013 |
The recurrence rate increases in patients with low histological grade or lymph node
metastases at diagnosis. The recurrence rate is even higher when the problem occurs
during wound healing after surgery.
|
Retrospective Study |
Calikapan et al.6 |
Marjolin ulcer of the scalp: intruder of a burn scar |
2008 |
Consistent with the literature, the histopathology of the tumors was squamous cell
carcinoma in most patients. Although rare, mesenchymal tumor is involved in 2 out
of 9 patients. The latency period of the tumor is inversely proportional to the age
at the time of the burn.
|
Cross-sectional study |
Serras et al.9 |
Melanoma Marjolin's ulcer in the hand: a case report |
2019 |
Female, 74 years old, with malignant melanoma resulting from a burn scar on the right
thenar eminence 14 years after the initial lesion. The lesion was excised, and a full-thickness
skin graft covered the defect. At 6 months postoperatively, there are no signs of
locoregional recurrence or systemic dissemination.
|
Case report |
Xiao et al.11 |
A review of 31 cases of Marjolin's ulcer on the scalp: Is it necessary to preventively
remove the scar?
|
2019 |
Of the 31 patients with MU on the scalp, the mean latency and post-ulceration period
was 42.9 years and 37.5 months, respectively. Among them, 30 patients were diagnosed
with cancer 5 years after the initial lesion, and 25 experienced a pre-ulceration
period of more than 20 years. A negative correlation was identified between the post-ulceration
period of the scalp MU and its pre-ulceration period.
|
|
Shen et al.12 |
Clinical characteristics and therapeutic analysis of 51 patients with Marjolin's ulcer |
2015 |
Among patients with squamous cell carcinoma, 30.23% had metastasis to the sentinel
lymph node, and 11.63% had distant metastasis. Among patients with melanoma, 66.67%
had sentinel lymph node metastases, and 33.33% had distant metastases.
|
Retrospective Study |
Costa et al.10 |
Epidemiology and treatment of pressure ulcers: experience of 77 cases |
2005 |
Forty-five patients with 77 ulcers were evaluated during this period. Regarding sex,
a 4:1 male predominance was found. 32.47% of the ulcers were located in the sacral
region, 32.47% in the trochanteric region, and 15.58% in the sciatic region. Mostly
young (mean age 34.78 years), with spinal cord injuries (100% of patients), victims
of firearm injuries (60% of patients), chronic (93.3%), and grade IV injuries ( 67.53%).
|
Prospective Study |
Chart 1 - Observational studies on Marjolin’s ulcer (UM).
The articles selected to compose our results were published between 2005 and 2019,
originating in China, the United States of America, South Korea, Turkey, Portugal,
and Brazil.
DISCUSSION
Marjolin’s ulcer is a rare and constantly aggressive disease. It develops in previously
damaged and chronically affected areas and undergoes malignant degeneration in 0.77
to 2% of wounds and scars, especially after burns2,5. According to Serras et al.9, the average latency time is 23 to 37 years, there is no distribution by race or
age, but it occurs, preferably in the fifth decade of life. It is more prevalent in
men and occurs mainly in the lower extremities, around 40%, followed by the upper
extremities, head, neck, and trunk 9,10.
The pathophysiology includes several etiological factors responsible for malignant
transformation. Decreased vascularity, combined with a weakened epithelium, creates
a susceptibility to wound chronification, one of the main mechanisms suggested since
the 1930s3.
MU can be diagnosed early through strict surveillance during the latency period3,11. When the wound healing period is prolonged due to lack of adequate treatment, it
can lead to loss of immune system cells and physiological events in a way that impairs
immune surveillance, resulting in the inability to recognize non-auto malignancy in
the early stages, which may lead to an aggressive condition prone to metastases3,5.
Chronic irritation and repetitive trauma in this malnourished area act as promoters
of degenerative changes, where there is a lack of collagen organization and impairment
of the vascular supply due to fibrosis, contributing to the weakening of the new epithelium
that will be formed and compromising the current immune system12.
Toxins released by tissue in necrosis can directly cause cell mutations5,9. Furthermore,
mutations in the genes responsible for cell division and apoptosis cause increased
carcinoma incidence in patients with MU5. However, once ulceration occurs, the irritating factor becomes indifferent due to
the rapidity with which the malignancy progresses, leading to advanced-stage diseases
faced by surgeons11.
The diagnosis begins with the history and clinical suspicion based on the characteristics
of the ulcer: raised, hardened edges, fetid odor, vegetative appearance, occasional
purulent discharge associated with pressure or venous ulcers, and burn scars. Collecting
samples from the center and edges of the ulcer is recommended for later histopathological
analysis and diagnostic confirmation5.
Furthermore, it is essential to deepen the patient’s history because poorly healed
burns during childhood may be the causal factor of the current injury12,13. There is a risk of metastases to regional lymph nodes, and in case of clinical suspicion
of lymph node involvement, these should be qualified for surgery. Sentinel lymph node
biopsy is highly sensitive and is recommended to identify metastases5.
With the possibility of involvement of noble structures, lesion recurrence, and metastases,
early diagnosis is of paramount importance14. The delay in seeking and receiving medical care and inadequate treatment due to
an error in diagnosing the wound postpones the therapeutic approach, which is essential
for a good prognosis9.
The SCC leads as the most common histological type and is formed by cells that mimic
those of the normal epidermis; however, with disorganized architecture, nuclear atypias,
and typical and atypical mitoses8,15. It is common to identify horny pearls, where keratin condensation occurs in the
center of cell clusters, an indication of good differentiation from squamous cell
carcinoma8. BCC is the second most common neoplasm7. It arises in the basal cells found in the deepest layer of the epidermis. Melanoma,
which ranks third in the incidence of MU, is a highly malignant tumor that originates
from melanocytes in the basal layer of the epidermis and infiltrates the dermis15,16.
Another important differential diagnosis is pseudoepitheliomatous or pseudocarcinomatous
hyperplasia17. It is a benign disease characterized by hyperplasia of the epidermis and adnexal
epithelium, which simulates SCC17. It is found in several heterogeneous diseases2,18. Also known as “invasive acanthosis” and “verrucous epidermal hyperplasia,” it can
be misinterpreted as SCC, especially in cases where the primary process located in
the dermis is not easily seen, or when the biopsy is superficial and does not include
a sufficient portion of the dermis18.
The use of non-surgical therapies is still controversial. The use of cisplatin, 5-fluorouracil,
and bleomycin showed partial or complete remissions2. However, the effects of chemotherapy and cytotoxic radiotherapy are still doubtful,
and there are divergences in the literature1,6. The radiotherapy effects are questioned due to the little vascularization around
the ulcerated tissue6; however, radiotherapy is often indicated in inoperable patients or as a post-surgical
consolidation treatment1,6. Among the indications for radiotherapy, there are:
metastasis from dead regional lymph nodes;
grade 3 lesions with positive lymph nodes after nodal dissection;
tumors greater than 10 cm in diameter and with positive lymph nodes after regional
lymph node dissection;
grade 3 lesions with tumor diameter greater than 10 cm and negative lymph nodes after
regional lymphatic dissection; and
head and neck lesions with positive lymph nodes after regional lymph node dissection5.
Currently, the most effective and used treatment is surgery1. Several authors suggest prophylactic lymph node dissection due to the aggressive
progression profile1,2. This is based on the histological grade of the tumor or the indication for sentinel
lymph node dissection and, according to recommendations, is performed only in clinically
positive lymph node chains or in cases of histologically positive lymph nodes after
fine needle aspiration puncture2. It is very commonly debated that positron emission computed tomography (PET-CT)
findings in combination with ultrasound-guided biopsy have a good accuracy rate for
searching for metastases in lymph nodes12.
Surgical intervention requires extensive tissue excision with margins of 2 cm4. In some cases, an extension of 5 cm from the edge of the wound is recommended1, possibly improving the prognosis by reducing post-surgical recurrence19. Radical excision is necessary because malignant transformation occurs mainly at
the edges of ulcers during secondary intention healing. The chance of a false-negative
biopsy, due to the focal nature of the malignant alteration, also suggests excisional
oncological clearance of the primary lesion, with horizontal safety margins of 2 to
4 cm and vertical margins close to uninvolved barrier structures2.
The depth of resection depends on the level of tumor cell invasion. The superficial
layer of the deep fascia, the muscle tissue, and the periosteum are structures possibly
affected by neoplastic cells1. In most cases, debridement at the facial level is a minimum requirement, and insufficient
resections can lead to impaired healing and recurrence2,19.
However, deep tissue and/or bone invasions make radical resection of the lesion difficult.
Amputation is indicated in cases of very extensive resections2,19. Deep muscle involvement demands greater excisions and may affect the periosteum
and cortical bone2,19. The structures’ excision is also indicated to avoid recurrence due to residual tumors1. Amputation is also considered in cases of joint infeasibility.
After ulcer resection, adequate repair and functional reconstruction should be instituted
to improve the patient’s quality of life through options such as skin grafting and
flaps20. Grafts are indicated in situations that demand monitoring of possible recurrences—flaps,
for covering important structures and maintaining function1,2. The microsurgical flap is indicated for cases with extensive resection, with the
possibility of postoperative radiotherapy20.
Quickly recognizing the signs of cancer recurrence after surgical excision is paramount
for a better prognosis. An active diagnosis through additional physical examinations,
general radiographs, computed tomography, and magnetic resonance imaging, among others,
may be necessary to obtain early confirmation of recurrence.
The triggering factors for recurrence are still poorly understood; however, the pre-surgical
histological grade of the carcinoma, healing disorders, and lymph node metastases
are factors that suggest a relationship with possible recurrence. The recurrence rate
is still being researched. Some studies have shown recurrence in 8 out of 12 patients,
4 to 5 months after surgery, with an average of 3 to 10 months4.
CONCLUSION
In short, UM is a rare but highly aggressive malignant neoplasm that needs to be better
studied and assisted. It has a wide differential diagnosis, which must be known so
that other hypotheses are discarded. The most effective treatment is surgery. Radiotherapy
may be indicated in specific preoperative cases or as postoperative adjuvant therapy,
and chemotherapy has not shown good results. In the initial stages, the malignant
tumor is subject to simple excision, and in late cases, resection, as it is wide,
can lead to high morbidity. That said, early diagnosis and adequate treatment are
the keys to the good evolution of MU.
1. Centro Universitário de Belo Horizonte, Belo Horizonte, MG, Brazil.
2. Universidade de Uberaba, Uberaba, MG, Brazil.
3. Faculdade de Ciências Médicas de Minas Gerais, Belo Horizonte, MG, Brazil.
4. Universidade Federal do Triângulo Mineiro, Uberaba, MG, Brazil.
Corresponding author: Nathália Nunes Rodovalho Alameda do Ingá, 785, apto 403, Vila da Serra, Nova Lima, MG, Brazil Zip code: 34006-042
E-mail: nathalia_nr@hotmail.com