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1.
Skin Res Technol ; 30(5): e13706, 2024 May.
Article in English | MEDLINE | ID: mdl-38721854

ABSTRACT

BACKGROUND: The incidence rates of cutaneous squamous cell carcinoma (cSCC) and basal cell carcinoma (BCC) skin cancers are rising, while the current diagnostic process is time-consuming. We describe the development of a novel approach to high-throughput sampling of tissue lipids using electroporation-based biopsy, termed e-biopsy. We report on the ability of the e-biopsy technique to harvest large amounts of lipids from human skin samples. MATERIALS AND METHODS: Here, 168 lipids were reliably identified from 12 patients providing a total of 13 samples. The extracted lipids were profiled with ultra-performance liquid chromatography and tandem mass spectrometry (UPLC-MS-MS) providing cSCC, BCC, and healthy skin lipidomic profiles. RESULTS: Comparative analysis identified 27 differentially expressed lipids (p < 0.05). The general profile trend is low diglycerides in both cSCC and BCC, high phospholipids in BCC, and high lyso-phospholipids in cSCC compared to healthy skin tissue samples. CONCLUSION: The results contribute to the growing body of knowledge that can potentially lead to novel insights into these skin cancers and demonstrate the potential of the e-biopsy technique for the analysis of lipidomic profiles of human skin tissues.


Subject(s)
Carcinoma, Basal Cell , Carcinoma, Squamous Cell , Electroporation , Lipidomics , Skin Neoplasms , Skin , Humans , Carcinoma, Basal Cell/pathology , Carcinoma, Basal Cell/metabolism , Carcinoma, Basal Cell/diagnosis , Skin Neoplasms/pathology , Skin Neoplasms/metabolism , Carcinoma, Squamous Cell/pathology , Carcinoma, Squamous Cell/metabolism , Carcinoma, Squamous Cell/chemistry , Lipidomics/methods , Biopsy , Skin/pathology , Skin/metabolism , Skin/chemistry , Female , Male , Electroporation/methods , Middle Aged , Aged , Lipids/analysis , Tandem Mass Spectrometry/methods
2.
Arch Dermatol Res ; 316(6): 282, 2024 May 25.
Article in English | MEDLINE | ID: mdl-38796611

ABSTRACT

Skin cancers are associated with a large number of genodermatoses. Existing knowledge and guidelines on the presentations of these genodermatoses focus disproportionately on White patients. Our goal is to identify notable characteristics in location, frequency, and severity of cutaneous findings along with the median age of skin cancers in skin-of-color (SOC) patients with skin-cancer-associated genodermatoses to improve diagnosis rates. We searched for genodermatoses on six databases. Each case report or case series was reviewed, including reports, published in English, containing adult patient descriptions. Duplicate manuscripts were removed using EndNote. The following case-level data were collected from the manuscripts: age, gender, patient country or region of origin, author country/continent of residence, skin cancer-related, and other key dermatologic features. 381 published articles, with a total of 578 SOC patients, met criteria for inclusion. SOC patients can present with fewer classic findings, such as a lower incidence of basal cell carcinomas (44%) in SOC Gorlin syndrome patients than palmar pits (66%) and mandibular cysts (66%). Differences between SOC populations were also noted, such as leukoplakia being more common in Asian dyskeratosis congenita patients (80%) in comparison to African dyskeratosis congenita patients (44%). SOC patients also have varying onset of skin cancer depending on the genodermatosis, from a median of 25 years of age in Rothmund-Thomson syndrome to 53 in Muir-Torre syndrome. In this review, SOC patients with genodermatoses can have varying presentations. Being cognizant of these characteristics may lead to earlier diagnosis and interventions to mitigate skin-cancer-related morbidity in SOC patients.


Subject(s)
Skin Neoplasms , Skin Pigmentation , Humans , Skin Neoplasms/epidemiology , Skin Neoplasms/diagnosis , Skin Neoplasms/pathology , Skin/pathology , Carcinoma, Basal Cell/epidemiology , Carcinoma, Basal Cell/pathology , Carcinoma, Basal Cell/diagnosis , Female , Male , Skin Diseases, Genetic/epidemiology , Skin Diseases, Genetic/diagnosis , Skin Diseases, Genetic/pathology
3.
Dermatol Online J ; 30(1)2024 Mar 15.
Article in English | MEDLINE | ID: mdl-38762857

ABSTRACT

Cutaneous basal cell carcinoma in situ is a recently proposed subtype of this skin cancer. It is characterized by either restriction of the tumor cells within the epidermis or the presence of tumor cells contiguous with the overlying epidermis that extend into the underlying dermis, or both. Importantly, cancer invasion-demonstrated by non-contiguous aggregates of basaloid tumor cells in the dermis-is not a feature of in situ basal cell carcinoma of the skin. A 63-year-old woman with cutaneous basal cell carcinoma in situ-superficial type that presented as an erythematous scaly plaque on her abdomen and a 61-year-old man with a cutaneous basal cell carcinoma in situ-fibroepithelioma type that presented as a flesh-colored smooth exophytic nodule on his back are reported. The characteristics of in situ basal cell carcinoma of the skin in these individuals are summarized. In conclusion, similar to other cutaneous malignant neoplasms-such as squamous cell carcinoma, malignant melanoma, and Merkel cell carcinoma-basal cell carcinoma of the skin can also present as an in situ cancer.


Subject(s)
Carcinoma, Basal Cell , Skin Neoplasms , Humans , Skin Neoplasms/pathology , Carcinoma, Basal Cell/pathology , Middle Aged , Female , Male , Carcinoma in Situ/pathology , Neoplasms, Fibroepithelial/pathology , Neoplasms, Fibroepithelial/diagnosis
4.
Dermatol Online J ; 30(1)2024 Mar 15.
Article in English | MEDLINE | ID: mdl-38762862

ABSTRACT

A 98-year-old woman presented with histologically confirmed locally advanced basal cell carcinoma of the face. A multidisciplinary approach excluded surgery because of the site near sensitive organs, extension, age, and comorbidities. Patient and caregivers declined radiotherapy considering the necessity of multiple hospital appointments. The patient was then placed on therapy with sonidegib, an oral inhibitor of the Hedgehog signaling pathway. There was a very rapid clinical response after only 28 days of treatment. The basal cell carcinoma improved progressively, with no adverse events reported. This case illustrates the efficacy and safety of this treatment in an advanced age patient. This treatment had a remarkably positive impact on quality of life, including that of the caregivers.


Subject(s)
Biphenyl Compounds , Carcinoma, Basal Cell , Pyridines , Skin Neoplasms , Humans , Female , Carcinoma, Basal Cell/drug therapy , Carcinoma, Basal Cell/pathology , Aged, 80 and over , Pyridines/therapeutic use , Pyridines/adverse effects , Skin Neoplasms/pathology , Skin Neoplasms/drug therapy , Biphenyl Compounds/therapeutic use , Antineoplastic Agents/therapeutic use , Antineoplastic Agents/adverse effects , Facial Neoplasms/drug therapy , Facial Neoplasms/pathology , Hedgehog Proteins/antagonists & inhibitors , Quality of Life
5.
Arch Dermatol Res ; 316(6): 210, 2024 May 24.
Article in English | MEDLINE | ID: mdl-38787399

ABSTRACT

Basal Cell Carcinoma (BCC) is the most prevalent skin cancer and continues to witness a surge in incidence rates. The categorization of BCC subtypes into low or high risk, guided by recurrence and invasiveness metrics, underscores the need for precise differentiation. While the punch biopsy remains the gold standard for diagnosis, its invasiveness prompts a need for non-invasive alternatives. Ultrasound (US) has emerged as a noteworthy candidate, gaining momentum in its potential to offer a less intrusive diagnostic approach. We conducted a systematic review regarding features of the high-risk subtypes of BCC on US. A thorough literature search of PubMed Medline, Embase, and CINAHL databases was conducted according to PRISMA guidelines and a total of nine studies meeting our inclusion criteria were included in this review. Evidence is still nascent but US features such as lesional shape, depth, hyperechoic spots, and color doppler may be helpful in differentiating high-risk BCC subtypes. However, further prospective studies with standardized interventions and outcome measures are required.


Subject(s)
Carcinoma, Basal Cell , Skin Neoplasms , Carcinoma, Basal Cell/diagnostic imaging , Carcinoma, Basal Cell/pathology , Carcinoma, Basal Cell/diagnosis , Carcinoma, Basal Cell/epidemiology , Humans , Skin Neoplasms/diagnostic imaging , Skin Neoplasms/pathology , Skin Neoplasms/diagnosis , Skin/diagnostic imaging , Skin/pathology , Ultrasonography, Doppler, Color/methods , Ultrasonography/methods , Biopsy
6.
Laryngorhinootologie ; 103(S 01): S100-S124, 2024 May.
Article in English, German | MEDLINE | ID: mdl-38697144

ABSTRACT

The interdisciplinary treatment of skin cancer in the head and neck area requires close collaboration between different specialist disciplines. The most common non-melanoma skin cancer tumor entities are cutaneous squamous cell carcinoma and basal cell carcinoma as well as their precursor lesions. One of the less common tumors is Merkel cell carcinoma, which also occurs primarily in light-exposed areas and, in contrast to squamous and basal cell carcinoma, is more likely to metastasize. Due to the low tendency of basal cell carcinoma as well as cutaneous squamous cell carcinoma to metastasize, a cure can often be achieved by surgery. If the tumor growth exceeds certain levels it may require collaboration between dermatology and otorhinolaryngology. The primary goal of this interdisciplinary collaboration is to achieve a functional, cosmetically and aesthetically acceptable result in addition to adequate tumor treatment. Depending on the stage of the tumor and the clinical course, a case may be discussed in an interdisciplinary tumor board in order to determine a personalised, appropriate and adequate treatment concept for each patient, including prevention, therapy and follow-up.


Subject(s)
Carcinoma, Basal Cell , Carcinoma, Squamous Cell , Interdisciplinary Communication , Skin Neoplasms , Skin Neoplasms/therapy , Skin Neoplasms/pathology , Skin Neoplasms/surgery , Humans , Carcinoma, Squamous Cell/therapy , Carcinoma, Squamous Cell/pathology , Carcinoma, Squamous Cell/surgery , Carcinoma, Basal Cell/therapy , Carcinoma, Basal Cell/pathology , Carcinoma, Basal Cell/surgery , Patient Care Team , Carcinoma, Merkel Cell/therapy , Carcinoma, Merkel Cell/pathology , Carcinoma, Merkel Cell/surgery , Intersectoral Collaboration , Neoplasm Staging
8.
Acta Derm Venereol ; 104: adv19678, 2024 May 07.
Article in English | MEDLINE | ID: mdl-38712969

ABSTRACT

In electrochemotherapy, permeabilization of the cell membrane by electric pulses increases the anti-tumour effect of chemotherapeutics. In calcium electroporation, chemotherapy is replaced by calcium chloride with obvious benefits. This study explores the effect and underlying mechanisms of calcium electroporation on basal cell carcinomas using either high- or low-frequency electroporation. Low-risk primary basal cell carcinomas were treated in local anaesthesia with intratumoral calcium chloride followed by electroporation with high (167 kHz) or low (5 kHz) frequencies. Non-complete responders were retreated after 3 months. The primary endpoint was tumour response 3 months after last calcium electroporation. Plasma membrane calcium ATPase was examined in various cell lines as plasma membrane calcium ATPase levels have been associated with calcium electroporation efficacy. Twenty-two out of 25 included patients complete the study and 7 of these (32%) achieved complete response at 3 months with no difference in efficacy between high- and low-frequency pulses. High-frequency calcium electroporation was significantly less painful (p=0.03). Plasma membrane calcium ATPase was increased 16-32-fold in basal cell carcinoma cell lines compared with 4 other cancer cell lines. Calcium electroporation for low-risk basal cell carcinomas does not fulfil the requirements of a new dermatological basal cell carcinoma treatment but may be useful as adjuvant treatment to surgery in more advanced basal cell carcinomas. The elevated PMCA levels in basal cell carcinomas may contribute to low efficacy.


Subject(s)
Carcinoma, Basal Cell , Electrochemotherapy , Skin Neoplasms , Humans , Carcinoma, Basal Cell/pathology , Carcinoma, Basal Cell/therapy , Skin Neoplasms/pathology , Skin Neoplasms/therapy , Male , Female , Middle Aged , Aged , Treatment Outcome , Electrochemotherapy/methods , Cell Line, Tumor , Calcium Chloride/administration & dosage , Aged, 80 and over , Plasma Membrane Calcium-Transporting ATPases/metabolism , Time Factors , Electroporation
10.
Arch Dermatol Res ; 316(6): 255, 2024 May 25.
Article in English | MEDLINE | ID: mdl-38795216

ABSTRACT

Since the scrotum is rarely exposed to sunlight, basal cell carcinoma (BCC) development in this area is an uncommon occurrence. As result, there is a scarcity of research covering this particular presentation, which poses a diagnostic and therapeutic challenge for clinicians. The objective of this systematic review is to provide a thorough overview of scrotal BCC, including a summary of its clinical characteristics, and microscopic subtypes. It also seeks to discuss the many techniques used in the management of this uncommon clinical presentation. Utilizing data from 1957 to October 2023, a systematic review of PubMed and Wiley Online Library was conducted to identify all cases of scrotal BCC with various presentations and managements. A total of 73 patients were included. The median patient age was 65.9 years (range 42 to 87). All studies were either case reports or case series. Our review shows that treatment with Mohs micrographic surgery (MMS), leads to a superior patient outcome based on anecdotal evidence in select cases. To deepen our understanding of Mohs surgery's efficacy in treating scrotal BCC, it is imperative to conduct more robust research in the form of randomized clinical trials.


Subject(s)
Carcinoma, Basal Cell , Mohs Surgery , Scrotum , Skin Neoplasms , Humans , Scrotum/pathology , Scrotum/surgery , Male , Carcinoma, Basal Cell/diagnosis , Carcinoma, Basal Cell/therapy , Carcinoma, Basal Cell/pathology , Carcinoma, Basal Cell/surgery , Skin Neoplasms/diagnosis , Skin Neoplasms/therapy , Skin Neoplasms/pathology , Skin Neoplasms/surgery , Aged , Middle Aged , Aged, 80 and over , Adult , Treatment Outcome
11.
Acta Derm Venereol ; 104: adv40112, 2024 May 27.
Article in English | MEDLINE | ID: mdl-38803206

ABSTRACT

Basal cell carcinoma (BCC) is a common skin cancer type and affected individuals are known to be at risk of developing multiple consecutive tumours. Research into BCC multiplicity has, thus far, been challenging, due to a lack of national registration. This registry-based cohort study aimed to analyse the occurrence of multiple BCCs in Sweden, and risk factors for subsequent primary BCCs. Data regarding all histopathologically verified, primary BCC tumours in Sweden from 2004 to 2017 was extracted from the Swedish BCC Registry. Risk of developing a subsequent BCC in relation to person-related factors was estimated with Cox regression analysis. Cumulative risk of BCC development after 1 or 3 earlier BCCs was estimated. In total, 39.9% of individuals with a registered BCC had at least 2 registered tumours. The risk of developing a subsequent BCC increased significantly in males, older age, and with residence in southern Sweden. The cumulative 5-year risk of developing an additional BCC after first diagnosis was approximately 30% in males and 27% in females and increased after multiple previous BCCs. This study showed the cumulative risk of a subsequent BCC to increase with a history of multiple BCCs, indicating the need for clinical surveillance in these individuals.


Subject(s)
Carcinoma, Basal Cell , Registries , Skin Neoplasms , Humans , Carcinoma, Basal Cell/epidemiology , Carcinoma, Basal Cell/pathology , Skin Neoplasms/epidemiology , Skin Neoplasms/pathology , Male , Female , Sweden/epidemiology , Middle Aged , Aged , Risk Factors , Adult , Aged, 80 and over , Neoplasms, Multiple Primary/epidemiology , Risk Assessment , Time Factors , Sex Factors , Age Factors , Young Adult , Hamartoma Syndrome, Multiple
13.
Acta Derm Venereol ; 104: adv18308, 2024 May 15.
Article in English | MEDLINE | ID: mdl-38751175

ABSTRACT

Photodynamic therapy is an approved treatment for primary, superficial, and small nodular basal cell carcinomas with a thickness of < 2 mm located on low-risk sites. Histologically verified basal cell carcinomas clinically assessed as suited for photodynamic therapy were included. The study aimed to investigate the agreement between clinical and histological assessments of basal cell carcinoma subtypes and thickness of tumours selected for photodynamic therapy with histopathological evaluation as a reference. A total of 343 tumours were included. The agreement between clinical and histological diagnosis of basal cell carcinoma subtype was 72% (p < 0.001). Clinical assessment of subtype had a sensitivity of 93% and specificity of 55% for superficial tumours and a sensitivity of 55% and specificity of 85% for nodular tumours. The mean ± SD thickness values by clinical and histological assessments were 0.95 ± 0.53 and 0.86 ± 0.75. The difference of 0.09 mm was statistically significant (p = 0.017), but not considered to be clinically relevant, although the differences between specific subgroups could be relevant. Among basal cell carcinomas clinically diagnosed as superficial, 91% were histologically consistent with the current photodynamic therapy criteria. The main results suggest that histopathological evaluation should precede photodynamic therapy to ensure selection of suitable basal cell carcinomas. In selected cases, the clinical diagnosis alone may be adequate before proceeding with photodynamic therapy.


Subject(s)
Carcinoma, Basal Cell , Photochemotherapy , Skin Neoplasms , Humans , Carcinoma, Basal Cell/pathology , Carcinoma, Basal Cell/drug therapy , Skin Neoplasms/pathology , Skin Neoplasms/drug therapy , Male , Female , Aged , Middle Aged , Aged, 80 and over , Predictive Value of Tests , Biopsy , Adult , Patient Selection , Photosensitizing Agents/therapeutic use , Retrospective Studies
14.
Med Oncol ; 41(6): 157, 2024 May 17.
Article in English | MEDLINE | ID: mdl-38758457

ABSTRACT

It has long been recognized that a history of skin cancer puts one at risk for additional primary skin cancers. However, more variable data exists for the risk of developing a non-cutaneous primary cancer following a diagnosis of skin cancer. The data are most variable for Basal Cell Carcinoma (BCC), the most common and least aggressive type of skin cancer. While early studies imply that BCC does not impart a larger risk of other primary non-cutaneous cancers, more recent studies with larger populations suggest otherwise. The cancers most significantly associated with BCC are lip, oropharyngeal, and salivary gland cancer. There is also burgeoning evidence to suggest a link between BCC and prostate, breast, and colorectal cancer, but more data are needed to draw a concrete conclusion. Squamous Cell Carcinoma (SCC), the second most common type of skin cancer, has a slightly more defined risk to other non-cutaneous primary malignancies. There is a notable link between SCC and non-Hodgkin's lymphoma (NHL), possibly due to immunosuppression. There is also an increased risk of other cancers derived from squamous epithelium following SCC, including oropharyngeal, lip, and salivary gland cancer. Some studies also suggest an increased risk of respiratory tract cancer following SCC, possibly due to shared risk factors. Melanoma, a more severe type of skin cancer, shows a well-defined risk of additional primary non-cutaneous malignancies. The most significant of these risks include NHL, thyroid cancer, prostate cancer, and breast cancer along with a host of other cancers. Each of these three main skin cancer types has a profile of genetic mutations that have also been linked to non-cutaneous malignancies. In this review, we discuss a selection of these genes to highlight the complex interplay between different tumorigenesis processes.


Subject(s)
Carcinoma, Basal Cell , Skin Neoplasms , Humans , Skin Neoplasms/epidemiology , Skin Neoplasms/pathology , Skin Neoplasms/etiology , Carcinoma, Basal Cell/epidemiology , Carcinoma, Basal Cell/etiology , Carcinoma, Basal Cell/pathology , Carcinoma, Squamous Cell/epidemiology , Carcinoma, Squamous Cell/etiology , Carcinoma, Squamous Cell/pathology , Melanoma/epidemiology , Melanoma/etiology , Melanoma/pathology , Risk Factors
16.
PLoS One ; 19(4): e0297531, 2024.
Article in English | MEDLINE | ID: mdl-38687774

ABSTRACT

Basal cell carcinoma (BCC) is highly curable by surgical excision or radiation. In rare cases, BCC can be locally destructive or difficult to surgically remove. Hedgehog inhibition (HHI) with vismodegib or sonidegib induces a 50-60% response rate. Long-term toxicity includes muscle spasms and weight loss leading to dose decreases. This retrospective chart review also investigates the impact of CoQ10 and calcium supplementation in patients treated with HHI drugs at a single academic medical center from 2012 to 2022. We reviewed the charts of adult patients diagnosed with locally advanced or metastatic BCC treated with vismodegib or sonidegib primarily for progression-free survival (PFS). Secondary objectives included overall survival, BCC-specific survival, time to and reasons for discontinuation, overall response rate, safety and tolerability, use of CoQ10 and calcium supplements, and insurance coverage. Of 55 patients assessable for outcome, 34 (61.8%) had an overall clinical benefit, with 25 (45.4%) having a complete response and 9 (16.3%) a partial response. Stable disease was seen in 14 (25.4%) and 7 (12.7%) progressed. Of the 34 patients who responded to treatment, 9 recurred. Patients who were rechallenged with HHI could respond again. The median overall BCC-specific survival rate at 5 years is 89%. Dose reductions or discontinuations for vismodegib and sonidegib occurred in 59% versus 24% of cases, or 30% versus 9% of cases, respectively. With CoQ10 and calcium supplementation, only 17% required a dose reduction versus 42% without. HHI is highly effective for treating advanced BCC but may require dosing decreases. Sonidegib was better tolerated than vismodegib. CoQ10 and calcium supplementation can effectively prevent muscle spasms.


Subject(s)
Anilides , Carcinoma, Basal Cell , Hedgehog Proteins , Pyridines , Ubiquinone/analogs & derivatives , Humans , Carcinoma, Basal Cell/drug therapy , Carcinoma, Basal Cell/pathology , Retrospective Studies , Male , Female , Middle Aged , Aged , Pyridines/therapeutic use , Pyridines/administration & dosage , Anilides/therapeutic use , Anilides/administration & dosage , Hedgehog Proteins/antagonists & inhibitors , Hedgehog Proteins/metabolism , Skin Neoplasms/drug therapy , Skin Neoplasms/pathology , Biphenyl Compounds/therapeutic use , Adult , Ubiquinone/therapeutic use , Ubiquinone/administration & dosage , Aged, 80 and over , Neoplasm Metastasis
17.
Med J Aust ; 220(9): 472-479, 2024 May 20.
Article in English | MEDLINE | ID: mdl-38685827

ABSTRACT

OBJECTIVES: To examine recent changes in the numbers of Medicare-subsidised keratinocyte cancer excisions, particularly for younger people exposed to primary prevention campaigns since the early 1980s. STUDY DESIGN: Retrospective cohort study; analysis of administrative data. SETTING, PARTICIPANTS: Analysis of Medicare Benefits Schedule (MBS) claims data for procedures related to the diagnosis and treatment of keratinocyte cancer in Australia, 2012-2021. MAIN OUTCOME MEASURES: Age-standardised rates for MBS-subsidised claims for first surgical squamous cell carcinoma (SCC) and basal cell carcinoma (BCC) excisions, Mohs surgery, surgical excisions of benign lesions, skin biopsies, and cryotherapy or serial curettage of premalignant and malignant lesions, overall, and by sex, state/territory, and age group; average annual percentage change in rate for time intervals determined by joinpoint regression. RESULTS: In men, the age-standardised rate of BCC/SCC excisions increased by 1.9% (95% confidence interval [CI], 1.4-2.4%) per year during 2012-2019 (from 2931 to 3371 per 100 000 men) and then declined by 3.8% (95% CI, 0.5-7.0%) per year during 2019-2021 (to 3152 per 100 000). In women, the age-standardised rate increased by 2.2% (95% CI, 1.7-2.8%) per year during 2012-2019 (from 1798 to 2093 per 100 000 women); the decline to 1967 excisions per 100 000 women in 2021 was not statistically significant. BCC/SCC excision rates declined for men under 55 years of age (by 1.0-3.4% per year) and women under 45 years of age (by 1.7-2.3% per year). Age-standardised biopsy rates increased during 2012-2021 in all age groups (by 2.8-6.9% per year). CONCLUSIONS: Rates of MBS-subsidised treatment for keratinocyte cancers increased during 2012-2019, but BCC/SCC treatment rates declined among younger Australians, who have probably been exposed to less sunlight than earlier generations because of public health interventions and population-wide lifestyle changes related to technology use.


Subject(s)
Carcinoma, Basal Cell , Carcinoma, Squamous Cell , Skin Neoplasms , Humans , Retrospective Studies , Male , Skin Neoplasms/pathology , Skin Neoplasms/epidemiology , Skin Neoplasms/surgery , Skin Neoplasms/therapy , Female , Australia/epidemiology , Carcinoma, Basal Cell/epidemiology , Carcinoma, Basal Cell/therapy , Carcinoma, Basal Cell/pathology , Carcinoma, Basal Cell/surgery , Middle Aged , Carcinoma, Squamous Cell/epidemiology , Carcinoma, Squamous Cell/pathology , Carcinoma, Squamous Cell/therapy , Aged , Adult , Keratinocytes/pathology , Aged, 80 and over , Mohs Surgery/statistics & numerical data , Young Adult , Cryotherapy/statistics & numerical data , Age Factors
18.
Am J Dermatopathol ; 46(5): 309-311, 2024 May 01.
Article in English | MEDLINE | ID: mdl-38574065

ABSTRACT

ABSTRACT: A collision tumor is an infrequent phenomenon characterized by the presence of 2 histologically distinct tumor types (either benign or malignant) occurring within the same specific anatomical site. We describe a rare case of co-occurrence of basal cell carcinoma and atypical fibroxanthoma presenting as a single lesion on the scalp in a 76-year-old man. The lesion was clinically suspicious for basal cell carcinoma and biopsied. Histologic examination showed 2 distinct tumors, one with basaloid cells and the other one with pleomorphic spindle cells colliding and growing together. Immunohistochemical stains were crucial in establishing the diagnosis. This presentation is exceedingly rare and requires additional evaluation for diagnosis.


Subject(s)
Carcinoma, Basal Cell , Histiocytoma, Benign Fibrous , Skin Neoplasms , Male , Humans , Aged , Histiocytoma, Benign Fibrous/pathology , Skin Neoplasms/diagnosis , Carcinoma, Basal Cell/pathology , Diagnosis, Differential , Scalp/pathology
19.
Anticancer Res ; 44(5): 2091-2094, 2024 May.
Article in English | MEDLINE | ID: mdl-38677729

ABSTRACT

BACKGROUND/AIM: Cathepsin G (CTSG) has been identified as an inhibitor of breast, bladder, and colorectal cancers. The G allele of the N125S (A/G, rs45567233) functional polymorphism of the CTSG gene confers increased serum CTSG activity and has been associated with cardiovascular and neurovascular diseases. This study examined the possible correlation between the pathogenesis of basal cell carcinoma (BCC) and the functional polymorphism CTSG N125S. PATIENTS AND METHODS: A total of 197 DNA samples were examined, comprising 98 BCC patients and 99 control samples of Greek origin. The CTSG N125S polymorphism was molecularly genotyped using PCR amplification, followed by enzyme digestion, and agarose gel electrophoresis of the amplified DNA fragments. RESULTS: There was no statistically significant difference in the genotypic and allelic frequencies between the patient and the control groups. CONCLUSION: There is no association between the CTSG N125S polymorphism and pathogenesis of BCC.


Subject(s)
Carcinoma, Basal Cell , Cathepsin G , Genetic Predisposition to Disease , Humans , Carcinoma, Basal Cell/genetics , Carcinoma, Basal Cell/pathology , Female , Male , Middle Aged , Cathepsin G/genetics , Aged , Skin Neoplasms/genetics , Skin Neoplasms/pathology , Gene Frequency , Case-Control Studies , Polymorphism, Single Nucleotide , Genotype , Aged, 80 and over , Adult , Risk Factors
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