| Literature DB >> 21129225 |
Abstract
BACKGROUND: Due to improved care, more and more children born with spina bifida in rural Kenya are surviving into adulthood. This improved survival has led to significant challenges in their lifestyles, especially the need to ensure pressure ulcer prevention and treatment. Malignant degeneration of pressure ulcers in spina bifida patients is very rare. The author describes the clinical presentation of two pressure ulcer carcinomas that are at variance from classical descriptions.Entities:
Mesh:
Year: 2010 PMID: 21129225 PMCID: PMC3014936 DOI: 10.1186/1477-7819-8-108
Source DB: PubMed Journal: World J Surg Oncol ISSN: 1477-7819 Impact factor: 2.754
Theories on Marjolin's ulcers [2-16]
| Theory | Proposed mechanism |
|---|---|
| Toxin theory | Toxins released from damaged tissues later lead to cellular mutations. |
| Chronic irritation theory | Chronic irritation with repeated attempts at re-epithelialization contributes to neoplastic initiation. |
| Traumatic epithelial elements implantation theory | Epithelial elements implanted into the dermis, lead to a foreign body response reaction and a disordered regenerative process. |
| Co-carcinogen theory | Chemical or trauma such as burn injury acts to 'stir' pre-existing but dormant neoplastic cells into proliferation. |
| Initiation and promotion theory | A two-step process that converts normal cells into malignant cells. In the initiation phase, normal cells become dormant neoplastic cells that may then be subsequently stimulated into neoplastic cells by a co-carcinogen such as infection, in the promotion phase. This theory overlaps with the co-carcinogen theory. |
| Immunologic privileged site theory | Burn scarring effectively obliterates lymphatics to injured area, preventing normal immunosurveillance and thus permitting neoplastic growth. These tumors initially grow slowly, but quickly overwhelm the immune system, metastasize and are rapidly fatal, once they break through the scar barrier. |
| Heredity theory | HLA DR4 is associated with cancer development and p53 gene abnormalities have been demonstrated in patients with Marjolin's ulcers. Further, |
| Ultraviolet rays theory | Ultraviolet rays theory - UV rays cause a reduction in Langerhans cell population leading to a reduction in cutaneous immuno-surveillance against developing malignancy and also cause p53 tumor suppressor gene alterations. |
| Environmental and genetic interaction theory | Attempts to explain the occurrence of 'Acute' Marjolin's ulcers. |
Figure 1Marjolin's ulcer with sinuses included within surgical excision margins. Note deep ulcer and benign appearance of ulcer edges.
Figure 2Marjolin's ulcer with sinuses extending into the thigh and labia majora. One sinus was found in the anus, and another in the vagina. Note benign appearance of ulcer margins surrounding a flat ulcer.
Prognostic factors in Marjolin's ulcers [19-24]
| PROGNOSIS | |||
|---|---|---|---|
| Clinical | Latency to malignancy | Less than 5 years | More than 5 years |
| Tumor location | Head, neck, upper extremeties | Lower limbs, trunk | |
| Tumor source | Post-burn, chronic osteomyelitis | Pressure sore carcinomas | |
| Tumor diameter | Smaller than 2 cm | 2 cm or more | |
| Tumor type | Exophytic | Infiltrative | |
| Metastases | None | Present | |
| Tumor recurrence | None | Present | |
| Histological | Degree of differentiation | Well differentiated | Moderately-well and poorly differentiated |
| Peritumoral T lymphocyte infiltration | Heavy | Scarce or absent | |
| Depth of dermal invasion | Superficial to reticular dermis | Reticular dermis or deeper | |
| Vertical tumor thickness | Less than 4 mm thick | 4 mm thick or more | |