Abstract:The risk of secondary solid malignancies is increased after allogeneic hematopoietic stem cell transplantation (HSCT). The risk starts at about 10 years after HSCT and continues even 20 years later. The most common secondary malignancies include squamous cell carcinoma of skin, genitourinary tract and oral cavity; lung and breast cancers. The use of total body irradiation or conditioning chemotherapy, chronic graft-versus-host disease and duration since HSCT can influence the risk of secondary solid malignanci… Show more
“…[ 10 – 13 ] The majority of solid malignancies following allogeneic HSCT are SCC affecting skin, genitourinary tract, and oral cavity. [ 14 ] Rizzo et al analyzed 28,874 allogeneic HSCT patients and reported that people with GVHD have 5 times the incidence of SCC compared with the general population. [ 10 ] In the past, some investigators suggested that patients with Fanconi anemia have a higher risk of head and neck SCC with poor survival.…”
Section: Discussionmentioning
confidence: 99%
“…Although the source of the patient's carcinoma in situ is unknown, it may be the result of multifactorial interactions, including genetic predisposition, individual behaviors, long-terms effects of chemotherapeutic drugs and radiation, and viral infections. [ 14 ]…”
Rationale:
Hematopoietic stem cell transplantation (HSCT) is the most effective treatment for the majority of patients who have malignant haemolytic disease. Although the success rate of HSCT has increased, the increasing number of cases suffering from secondary solid malignancies after HSCT has attracted more interest recently.
Patient concerns:
A 16-year-old female patient from China presented with a crusty and painful lesion on the left buccal mucosa with a history of chronic graft-versus-host disease following allogeneic HSCT for acute myeloid leukaemia.
Diagnosis:
An incisional biopsy of the lesion showed stratified squamous epithelium mucosa with severe dysplasia (carcinoma in situ). Subsequently, a wide local excision was performed and histological examination revealed early infiltrating squamous epithelial mucosa (carcinoma in situ).
Interventions:
She was being treated in the oral and maxillofacial surgery clinic with an incisional biopsy of the left buccal mucosa. She also received a wide local excision.
Outcomes:
Follow-up for 4 years showed no recurrence.
Lessons:
This case helps raise awareness of the diagnosis of oral symptoms in young patients after HSCT. Due to the increasing application of HSCT, raising awareness in oral and dental physicians may be required to improve long-term clinical outcome of patients who underwent HSCT.
“…[ 10 – 13 ] The majority of solid malignancies following allogeneic HSCT are SCC affecting skin, genitourinary tract, and oral cavity. [ 14 ] Rizzo et al analyzed 28,874 allogeneic HSCT patients and reported that people with GVHD have 5 times the incidence of SCC compared with the general population. [ 10 ] In the past, some investigators suggested that patients with Fanconi anemia have a higher risk of head and neck SCC with poor survival.…”
Section: Discussionmentioning
confidence: 99%
“…Although the source of the patient's carcinoma in situ is unknown, it may be the result of multifactorial interactions, including genetic predisposition, individual behaviors, long-terms effects of chemotherapeutic drugs and radiation, and viral infections. [ 14 ]…”
Rationale:
Hematopoietic stem cell transplantation (HSCT) is the most effective treatment for the majority of patients who have malignant haemolytic disease. Although the success rate of HSCT has increased, the increasing number of cases suffering from secondary solid malignancies after HSCT has attracted more interest recently.
Patient concerns:
A 16-year-old female patient from China presented with a crusty and painful lesion on the left buccal mucosa with a history of chronic graft-versus-host disease following allogeneic HSCT for acute myeloid leukaemia.
Diagnosis:
An incisional biopsy of the lesion showed stratified squamous epithelium mucosa with severe dysplasia (carcinoma in situ). Subsequently, a wide local excision was performed and histological examination revealed early infiltrating squamous epithelial mucosa (carcinoma in situ).
Interventions:
She was being treated in the oral and maxillofacial surgery clinic with an incisional biopsy of the left buccal mucosa. She also received a wide local excision.
Outcomes:
Follow-up for 4 years showed no recurrence.
Lessons:
This case helps raise awareness of the diagnosis of oral symptoms in young patients after HSCT. Due to the increasing application of HSCT, raising awareness in oral and dental physicians may be required to improve long-term clinical outcome of patients who underwent HSCT.
“…Similarly, Apel et al identified 7.4% of de novo non‐skin malignancies in kidney transplant recipients that represented breast cancer . The same is true for hematopoietic stem cell transplant recipients, whose risk for secondary solid malignancies is higher, with breast cancer being one of the most common .…”
“…HSCT conditioning regimens, like chemotherapy and/or radiotherapy, can play an important role in malignant transformation . Also, the risk of developing oral cancer after the transplantation increases over time . The incidence of subsequent solid tumors after HSCT is approximately 1% and 19%, whereas the rates at 10 years are between 2.2% and 6.1% .…”
Section: Risk Factors and Prevention Of Oscc In Famentioning
confidence: 99%
“…43 Also, the risk of developing oral cancer after the transplantation increases over time. 44 The incidence of subsequent solid tumors after HSCT is approximately 1% and 19%, whereas the rates at 10 years are between 2.2% and 6.1%. 45 In addition, individuals with FA who previously received HSCT had a 4.4-fold higher risk of developing HNSCC at a younger age.…”
Section: Risk Factors and Prevention Of Oscc In Famentioning
Fanconi anemia (FA) is a rare inherited genetic condition that may lead to bone marrow failure, leukemia, and/or solid tumors. It is caused by the loss of function of at least 1 gene of the FA/BRCA pathway, which is necessary for DNA repair. Patients with FA have a 200‐fold to 1000‐fold risk of developing head and neck cancer, mainly oral squamous cell carcinoma (OSCC), and of doing so at a much younger age than individuals within the general population. Also, patients who have FA with OSCC have poor overall survival rates, reinforcing the necessity to detect OSCC early. The scope of the current review is to provide an update on OSCC in patients with FA.
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