Next Article in Journal
Needs of Lung Cancer Patients Receiving Immunotherapy and Acceptance of Digital and Sensor-Based Scenarios for Monitoring Symptoms at Home—A Qualitative-Explorative Study
Next Article in Special Issue
Investigating PTG in Cancer Patients: The Role of Time Dimension in the Experience of Personal Growth
Previous Article in Journal
A Non-Randomized Pilot Study on the Benefits of Baby Swimming on Motor Development
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Early Diagnosis of Melanoma and Breast Cancer in Women: Influence of Body Image Perception

by
Jessica Ranieri
1,
Dina Di Giacomo
1,
Federica Guerra
1,
Eleonora Cilli
1,
Alessandra Martelli
2,
Valeria Ciciarelli
3,4,
Alessandra Ventura
3,4 and
Maria Concetta Fargnoli
3,4,*
1
Department of Life, Health and Environmental Sciences (MESVA), University of L’Aquila, P.le S. Tommasi 1, 67010 L’Aquila, Italy
2
Campus Universitario “Aurelio Saliceti”, University of Teramo, Via Renato Balzarini 1, 64100 Teramo, Italy
3
UOSD Oncological and General Dermatology, Via Lorenzo Natali 1, 67100 Padova, Italy
4
Department of Biotechnological and Applied Clinical Sciences (DISCAB), University of L’Aquila, Via Vetoio, 67100 L’Aquila, Italy
*
Author to whom correspondence should be addressed.
Int. J. Environ. Res. Public Health 2022, 19(15), 9264; https://doi.org/10.3390/ijerph19159264
Submission received: 2 June 2022 / Revised: 23 July 2022 / Accepted: 25 July 2022 / Published: 28 July 2022

Abstract

:
The diagnosis of melanoma and breast cancer may impact many aspects of life with significant reductions in emotional functioning and quality of life. The aim of the study was to analyze the emotional traits of female patients with oncological in early-stage diagnosis, investigating predictors for psychological distress and analyzing body image perception. An observational study was conducted, A sample of 84 female cancer patients (age range 30–55 years) with melanoma (n = 42) and breast cancer diagnosis (n = 42). The examined emotional variables were psychological distress; depression, stress, and anxiety; metacognitions; and body self-perception. Findings showed higher psychological distress in breast cancer than in melanoma patients (p = 0.00), which was related to lower positive self-perception of body image (p = 0.03). Furthermore, psychological distress was negatively correlated with consequences of clinical treatment on body image, and low well-being affected the social interaction and well-being with own body. There was no significant difference between cancer staging and timing from diagnosis. Prevention and therapeutic psychological protocols might be adapted and tailored to the unmet needs of the patients in medical treatments to promote and enhance the Quality of Life in survivorship.

1. Introduction

Acceleration in psychosocial research efforts over the past 5 years is clear; however, this has not been enough to define psychological aspects and emotional trends of early cancer (melanoma/breast) stage female patients during the clinical trajectory. Currently, new medical treatments are being offered promising long survivorship as a chronic life-threatening disease, however, most of randomized clinical trials are focused on medical treatment outcomes of cancer rather than psychosocial ones. Psychosocial research and practice have failed to keep pace with advances in the medical management of the disease [1,2,3,4,5].
Negative emotional reactions to stressful life events are a normal short-term emotional–behavioral response to threat; anger and fear are not a sign of psychopathological disorder [2,4]. Melanoma and breast cancer may have a considerable impact on patients’ lives including their health-related quality of life. Moreover, psychological responses to diagnosis and treatments may vary substantially over time and according to clinical aspects of the healthcare pathway. Throughout the diagnostic process and survivorship, patients with melanoma/breast cancer report significant reductions in psychological well-being and quality of life, including greater pain and fatigue, insomnia, and greater interference of stressors (physical and emotional) on social activities [1,2,3,4,5,6].
The antecedents and contributing factors to distress and other psychosocial outcomes are largely unexplored. Furthermore, a clear framework for adaptation and effective coping in the context of early-stage cancer is not defined to identify patients at risk of negative psychosocial outcomes in order to structure personalized interventions. Kasparian’s contribution [7] has highlighted oncological patients’ significant psychosocial challenges and consequences of having melanoma. A diagnosis of melanoma may impact all aspects of life. The primary negative impact of melanoma is on an individual personal level (life expectation, body image, self-esteem, well-being); the secondary effect is on social relationships (sociality, work performance, sexuality, family roles).
The psychological distress evoked by a cancer diagnosis, long-lasting threatening survivorship, and outcome uncertainty may impact negatively on patient compliance to medical treatment and win back to everyday life.
Several studies have focused on melanoma and breast cancer linked mental health issues, detecting negative psychological aspects and emotional dimensions. However, a few studies have analyzed the mental health management in early-stage melanoma/breast cancer patients, pointing out body self-perception factors to figure out how the adaptive change is related to oncological therapy, referring to image perception. Assessing body self-perception and identifying its features might serve as a suitable indicator of the cumulative health deterioration that may contribute to a poorer quality of life.
The study aimed to investigate the emotional traits of female patients with early-stage melanoma and breast cancer diagnosis, analyzing body image perception. Breast cancer and melanoma were selected for this study because they have an impact on the physical perception and body image of women, making them relevant for Quality of Life and well-being aspects in survivorship [8,9].
The objective of the study was to analyze the dynamics of psychological dimensions in early-stage breast cancer and melanoma patients by a long follow-up (1–5 years after primary medical treatment); we examined the metacognition thinking, emotional traits, and body self-perception to verify the outcome on well-being.

2. Materials and Methods

2.1. Ethics Approval

This study was approved by the Institutional Review Board of the University of L’Aquila, Italy (Prot. N° 16,372/2019). Written Informed Consent was obtained from each participant, and all procedures were in accordance with the Declaration of Helsinki.

2.2. Participants

Participants were n = 84 female patients aged 30–55 years old (mean age 42.2, ±8.3), living in central Italy distributed in 2 groups: (a) Melanoma group (Mg) composed of n = 42 patients with melanoma diagnosis (Stage 0-II) and (b) Breast cancer group (Bg) composed of n = 42 patients with a breast cancer diagnosis (Stage 0-II). All patients had an early-stage diagnosis by early screening.
Eligible participants have been selected from medical records and approached to be enrolled in the study at S. Salvatore Hospital in L’Aquila (IT) during subsequent scheduled appointments by medical protocol. We contacted 114 eligible patients, of whom 84 provided informed consent; 28 patients did not consent to participate in the experimental protocol; whereas two patients signed the informed consent form, but at the first session, they declined further involvement (dropped out).
Inclusion criteria included: (a) 30–55 years old; (b) no cancer recurrence or second cancer; and (c) timing of disease covering a range of disease 0–120 months from the diagnosis of melanoma/breast cancer; (d) drop-outs long-standing by relevant chemotherapy side effects.
Participants were eligible to enrol in the study if they had a breast cancer diagnosis or melanoma and followed a clinical path within 24 months following diagnosis, and after surgical intervention and/or treatment with adjuvant chemotherapy, radiation therapy, or both, for stages 0-II cancer.
Medical staff applied the TNM classification of Malignant Tumours (Tumor Nodes Metastasis, TNM), a cancer staging system developed by the American Joint Committee on Cancer and the Union for International Cancer Control (UICC), to classify the cancer stage of patients.
The recruitment process is described in Figure 1. Demographic characteristics of the participants are reported in Table 1.

2.3. Measurement

2.3.1. Sociodemographic Variables

Sociodemographic data were collected. First, demographic data were provided via the self-report of patients (age, having children, marital status, education, occupation). Second, clinical data were obtained from the patients’ medical records regarding melanoma and breast cancer stage, diagnosis timing, surgical treatments, and pharmacological therapies.

2.3.2. Psychological Tests

The psychological battery was composed of n 4 standardized questionnaires aimed to measure psychological distress (Psychological Distress Inventory) to assess signs of anxiety, depression, and stress (Depression Anxiety Stress Scale 21), and to detect metacogni-tive thinking (Metacognition Questionnaire 30).
Psychological Distress Inventory (PDI) [10]: this is a standardized 5-point self-administered 13 item-questionnaire developed to measure the level of psychological distress caused by cancer. The standard score indicates the presence/absence of psychological distress. The internal reliability was good (α = 0.86).
Depression Anxiety Stress Scales-21 (DASS-21) [11]: DASS-21 is a standardized 21-item self-report questionnaire assessing three dimensions (7 items per subscale): depression, anxiety, and stress. Patients are asked to score every item on a scale from 0 (did not apply to me at all) to 3 (applied to me very much). Sum scores are computed by adding up the scores on the items per (sub)scale and multiplying them by a factor of 2. Sum scores for each of the subscales may range between 0 and 42. The internal reliability was good (α = 0.78).
Metacognition Questionnaire-30 (MCQ-30) [12]: it is a standardized self-report assessing a range of metacognitive beliefs and processes relevant to the vulnerability and maintenance of psychological disorders. The items are rated on a 4-point Likert scale from 1 (do not agree) to 4 (completely agree). The items are grouped into five subscales: (a) Cognitive Confidence (CC), (b) Positive Beliefs about Worry (POS), (c) Cognitive Self-Consciousness (CSC), (d) Negative Beliefs about Uncontrollability and Danger (NEG), (e) Need to Control Thoughts (NC). The MCQ-30 has good internal consistency, as do its five subscales. The internal reliability was good (α = 0.80).
Body Self-perception questionnaire (BSPq): It is an ad hoc questionnaire consisting of 16 items aimed to measure three domains of body image perception: (a) consequences of clinical treatment on body image (Treatment Consequences on Body Image, TCBI); (b) well-being in social interactions (Social Wellness, SW), (c) and well-being with your body (Physical Feeling, PF). Responses are based on a 4-point Likert scale. The higher the scores better body self-perception. The pilot study previously conducted showed good reliability. The internal reliability was good (α = 0.82).

2.4. Procedure

Medical staff in the Oncological Dermatology Division (Director Prof. M.C. Fargnoli) identified eligible patients. All participants were then enrolled during clinical follow-up according to medical protocol. Written informed consent was obtained at the time of enrolment. Trained clinical psychologists (blinded to the aim of the study) conducted the psychological evaluations, lasting 40 min in a dedicated room. The participants filled out digital versions of the questionnaires; the psychological evaluation lasted 30 min. Participants were recruited on an outpatient basis during their scheduled medical follow-ups. Data were collected anonymously.

2.5. Study Design

We conducted an observational study to evaluate the emotional traits, body self-perception, and metacognitions in melanoma and breast cancer patients.

2.6. Statistical Analysis

Descriptive statistics were calculated for baseline characteristics and outcome measures. Multivariate analysis of variance (MANOVA) was conducted to detect the statistical significance of the overall differences across the examined psychological variables. Then, Pearson r correlations were applied. Statistical analyses were performed using the Jamovi 1.6.10.0 with a fixed α-value ≤ 0.05.

3. Results

Analyzing the sociodemographic data, breast cancer and melanoma patients did not differ significantly by age (t = 112, p = 0.27), education (Chi2 = 1.64, p = 0.44), and marital status (Chi2 = 0.66, p = 0.42), or perceived standard of living (Chi2 = 0.92, p = 0.63) at 1 month post-diagnosis (T1, see Table 1). Participants resulted homogeneous in demographic data.
In Table 2, we reported clinical treatments. As expected, treatments differed between the types of cancer.
Almost all breast cancer patients were treated with surgery (66.6% lumpectomy and 30.9% mastectomy) and radiotherapy; 38% of them received hormonal therapy, and half of them received chemotherapy. Differently, melanoma patients received surgical excision and no pharmacological therapy.
Both groups (Mg and Bg) showed no signs of anxiety, depression, or stress comparing raw score and cut-off (DASS-21 Anxiety score < 7, DASS-21 Depression score < 9, DASS-21 Stress score < 14). Only Bg showed psychological distress (PDI score > 25). Table 3 reported the raw scores.
Then, MANOVA statistical analyses (3 × 2) were conducted, comparing emotional traits (MCQ, PDI, BPS) and groups (Bg and Mg). Mg evidenced significant positive emotional traits than Bg: Bg showed higher psychological distress (p = 0.00), whereas Mg showed better Body Image Perception (p = 0.03), in the Impact of Treatment Consequences on Body Image index (p = 0.01) and on social wellness index (p = 0.04) (see Figure 2).
Further, we examined the relationship between body image perception (BSPq: TCBI, SW, PF) and psychological dimension (PDI), as well as metacognitive beliefs (MCQ-30: POS, NEG, CC, NC, CSC). We conducted a Pearson’s correlation analysis: the results are summarized in Figure 3. Psychological distress (PDI) was negatively correlated with consequences of clinical treatment on body image (TCBI) (r = −0.5; p < 0.001), well-being in social interaction (SW) (r = −0.4; p < 0.001), and well-being with own body (PF) (r = −0.5; p < 0.001). Then, metacognitive beliefs (MCQ-30) were negatively correlated with body image perception (BSPq): significant correlations emerged between TCBI and NEG (r = −0.5; p < 0.001), CC (r = −0.4; p < 0.001), NC (r =−0.2; p = 0.01); between SW and NEG (r = −0.3; p = 0.003), CC (r = −0.3; p = 0.005), NC (r =−0.2; p = 0.02); between PF and NEG (r = −0.2; p = 0.001), CC (r = −0.4; p < 0.001). Last, timing from diagnosis (time range 0–120 months) resulted in no significance.

4. Discussion

The aim of the study was to analyze the emotional traits of female patients with early-stage breast cancer and melanoma diagnosis, verifying the diagnosis impact on body image perception; in particular, the focus of the study was to define the predictive factor of psychological stress by metacognition thinking, emotional traits and body self-perception on the younger sample (range age 30–55 years).
According to the emerging literature on the well-being of younger cancer patients in survivorship [11,12,13,14,15,16], our findings showed that young women with melanoma/breast cancer resilient, as in our sample, showed no signs of mood disorders or psychopathological conditions.
According to Bourdon’s suggestions [17], melanoma patients showed fewer negative physical and social consequences than breast cancer patients, which decreased their body image self-perception as physical and role functioning, experiencing more extensive and painful treatment. Breast cancer patients have higher psychological distress and low body image perception than melanoma patients; it is interesting to highlight the age effect across patient groups, with younger patients seeming to better impact the disease pathway.
Our study shows that early-stage melanoma patients represent an oncological target with a better adaptability and management of their own body in the post-diagnosis than breast cancer patients. Early screening, as an effective tool for the early diagnosis of melanoma, favors not only less invasive clinical treatments but also a greater awareness of one’s body with a better management of it in the post-diagnosis, thus laying down for a better quality of life and well-being during survivorship.
Taking into account breast cancer patients’ performance, the diagnosis represents a stressor not only for illness management but even for physical perception, impacting significantly on the psychological dimensions of body image. Our finding evidenced significant relations of body image perception with emotion regulation and metacognitive beliefs of breast cancer women: low body self-perception appeared related to high psychological distress; moreover, high body self-perception was related to lower levels of unhelpful metacognitions.
Our findings confirmed the investigated largely negative impact of cancer diagnosis [2,5,8,13,14,15,16] and contributed to emerging research topics regarding the clinical implication of early diagnosis at a younger age (in this case in the female population), detecting the high relevance of clinical psychological interventions among medical and pharmacological solutions in primary treatments. While cancer treatment is being planned, all women should be informed about the possible side-effects of treatment on body image. Despite that the psychological impact of cancer on body image in young women has been identified, self-perception issues are not systematically addressed in the comprehensive care to these patients.
Emotional and metacognition screening and body image perception of BC and melanomal patients should be encouraged to prevent and/or reinforce by tailored psychological (integrated) treatment to enhance metacognitive beliefs for a better mantainence of a good level of body image perception.
This study has some limitations. First, this study is an observational study, which is difficult to determine the causal relationships; further follow-up studies are needed. The psychological battery is composed of self-report measures of distress symptoms and metacognitive thinking and are not measures of their clinical indicators. Further, the relatively small sample size limits the generalizability of our findings regarding regaining a normal life after the clinical pathway.
In conclusion, our study evidenced BC women had lower well-being compared to women with melanoma in survivorship. The study suggested that psychological support in primary treatments should be tailored to enhance the recovery of well-being and Quality of Life in survivors. Priority for psychological treatments should be adapted to the unmet needs of the patients in the medical pathway and for their own life perspectives. Last, our finding highlighted the need for regular screening of psychological distress even in patients with an early cancer diagnosis and in the case of long-term follow-up.

Author Contributions

The study was conceptualized and designed by D.D.G. and M.C.F. Author D.D.G. had full access to all of the data in the study and take responsibility for the integrity of the data and the accuracy of the data analysis. Authors F.G., J.R. and E.C. collected data, conducted statistical analysis and the interpretation of data. Author D.D.G. wrote the first draft of the article. V.C., A.M. and A.V. enrolled study participants. Author M.C.F. supervised the project. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Institutional Review Board Statement

This study was approved by the Institutional Review Board of the University of L’Aquila, Italy (Prot. N° 16,372/2019).

Informed Consent Statement

Written Informed Consent was obtained from each participant and all procedures were in accordance with the Declaration of Helsinki.

Data Availability Statement

Not applicable.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Al-Shakhli, H.; Harcourt, D.; Kenealy, J. Psychological distress surrounding diagnosis of malignant and nonmalignant skin lesions at a pigmented lesion clinic. J. Plast. Reconstr. Aesthet. Surg. 2006, 59, 479–486. [Google Scholar] [CrossRef] [PubMed]
  2. Hamama-Raz, Y.; Solomon, Z.; Schachter, J.; Azizi, E. Objective and subjective stressors and the psychological adjustment of melanoma survivors. Psycho-Oncology 2007, 16, 287–294. [Google Scholar] [CrossRef] [PubMed]
  3. Kasparian, N.A.; Butow, P.N.; Meiser, B.; Mann, G.J. High- and average-risk individuals’ beliefs about, and perceptions of, malignant melanoma: An Australian perspective. Psycho-Oncology 2008, 17, 270–279. [Google Scholar] [CrossRef] [PubMed]
  4. Cornish, D.; Holterhues, C.; van de Poll-Franse, L.V.; Coebergh, J.W.; Nijsten, T. A systematic review of health-related quality of life in cutaneous melanoma. Ann. Oncol. 2009, 20, vi51–vi58. [Google Scholar] [CrossRef] [PubMed]
  5. Ranieri, J.; Guerra, F.; Perilli, E.; Cilli, E.; Di Giacomo, D. Metacognitions and quality of life in survivorship after breast cancer diagnosis. Riv. Psichiatr. 2021, 56, 217–222. [Google Scholar] [PubMed]
  6. Di Giacomo, D.; Ranieri, J.; Guerra, F.; Cilli, E.; Ciciarelli, V.; Ventura, A.; Fargnoli, M.C. Early stage melanoma diagnosis and mental health-related: Emotional influence of body self-perception. J. Affect. Disord. Rep. 2021, 6, 100188. [Google Scholar] [CrossRef]
  7. Kasparian, N.A. Psychological stress and melanoma: Are we meeting our patients’ psychological needs? Clin. Dermatol. 2013, 31, 41–46. [Google Scholar] [CrossRef] [PubMed]
  8. Lehto, U.S.; Ojanen, M.; Kellokumpu-Lehtinen, P. Predictors of quality of life in newly diagnosed melanoma and breast cancer patients. Ann. Oncol. 2005, 16, 805–816. [Google Scholar] [CrossRef] [PubMed]
  9. Engel, J.; Schlesinger-Raab, A.; Emeny, R.; Hölzel, D.; Schubert-Fritschle, G. Quality of life in women with localised breast cancer or malignant melanoma two years after initial treatment: A comparison. Int. J. Behav. Med. 2014, 21, 478–486. [Google Scholar] [CrossRef] [PubMed]
  10. Morasso, G.; Costantini, M.; Baracco, G.; Borreani, C.; Capelli, M. Assessing psychological distress in cancer patients: Validation of a self-administered questionnaire. Oncology 1996, 53, 295–302. [Google Scholar] [CrossRef] [PubMed]
  11. Lovibond, S.H.; Lovibond, P.F. Manual for the Depression Anxiety & Stress Scales, 2nd ed.; Psychology Foundation: Sydney, Australia, 1995. [Google Scholar]
  12. Wells, A.; Cartwright-Hatton, S. A short form of the Metacognitions Questionnaire: Properties of the MCQ-30. Behav. Res. Ther. 2004, 42, 385–396. [Google Scholar] [CrossRef]
  13. Di Giacomo, D.; Ranieri, J.; Perilli, E.; Cannita, K.; Passafiume, D.; Ficorella, C. Psychological impact of clinical treatment after breast cancer diagnosis in younger patients (38–50 age range): An explorative 3-year observational study. Neurol. Psychiatry Brain Res. 2019, 32, 85–90. [Google Scholar] [CrossRef]
  14. Martino, M.L.; Lemmo, D.; Gargiulo, A. A review of psychological impact of breast cancer in women below 50 years old. Health Care Women Int. 2021, 42, 1066–1085. [Google Scholar] [CrossRef] [PubMed]
  15. Martino, M.L.; Gargiulo, A.; Lemmo, D.; Dolce, P.; Barberio, D.; Abate, V.; Avino, F.; Tortoriello, R. Longitudinal effect of emotional processing on psychological symptoms in women under 50 with breast cancer. Health Psychol. Open 2019, 6, 2055102919844501. [Google Scholar] [CrossRef] [PubMed]
  16. Martino, M.L.; Lemmo, D.; Gargiulo, A.; Barberio, D.; Abate, V.; Avino, F.; Tortoriello, R. Underfifty Women and Breast Cancer: Narrative Markers of Meaning-Making in Traumatic Experience. Front. Psychol. 2019, 10, 618. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  17. Bourdon, M.; Blanchin, M.; Tessier, P.; Campone, M.; Quéreux, G.; Dravet, F.; Sébille, V.; Bonnaud-Antignac, A. Changes in quality of life after a diagnosis of cancer: A 2-year study comparing breast cancer and melanoma patients. Qual. Life Res. 2016, 25, 1969–1979. [Google Scholar] [CrossRef] [PubMed]
Figure 1. Flowchart of the participants.
Figure 1. Flowchart of the participants.
Ijerph 19 09264 g001
Figure 2. Psychological distress and self-body perception representation of both Bg and Mg groups.
Figure 2. Psychological distress and self-body perception representation of both Bg and Mg groups.
Ijerph 19 09264 g002
Figure 3. Pearson r correlations between PDI, BSPq, and MCQ-30 scores for the sample.
Figure 3. Pearson r correlations between PDI, BSPq, and MCQ-30 scores for the sample.
Ijerph 19 09264 g003
Table 1. Sociodemographic data of participants.
Table 1. Sociodemographic data of participants.
Age, YearsBreast Group
(Mean Age 45.3, Sd ± 1.5)
Melanoma Group
(Mean Age 45.5, Sd ± 2.5)
Relationship status
Married/living with partner80.9%78.5%
Single19.0%21.4%
Education
Not graduate19.0%4.7%
High school52.3%64.2%
Graduation28.5%30.9%
Occupation
Housewife27.9%23.8%
Employed53.5%57.1%
Self-employed17.4%19.0%
TNM Cancer stage
047.6%40.4%
I28.5%57.1%
II23.8%2.3%
Diagnosis Timing
T0 (0–12 months)30.9%21.4%
T1 (13–60 months)57.1%45.2%
T2 (>61 months)11.9%33.3%
Table 2. Clinical treatments for patients with breast cancer and melanoma.
Table 2. Clinical treatments for patients with breast cancer and melanoma.
Melanoma GroupBreast Cancer Group
Surgery
Excision(n = 42) 100%-
Lumpectomy-(n = 29) 69.0%
Mastectomy-(n = 13) 30.9%
Pharmacological therapy *
No treatment(n = 42) 100%(n = 3) 7.1%
Chemotherapy-(n = 22) 52.3%
Hormonal therapy-(n = 16) 38.0%
* Chemotherapy and hormonal therapy are not mutually excluded.
Table 3. The raw score (mean and standard deviations) of participants in the psychological evaluation.
Table 3. The raw score (mean and standard deviations) of participants in the psychological evaluation.
TestBreast Cancer GroupMelanoma Group
MSdMSd
MCQ-3058.510.360.712.4
POS9.03.010.23.4
NEG13.13.513.23.3
CC10.63.810.43.4
NC11.03.411.63.2
CSC14.63.115.23.6
PDI29.28.823.35.4
BSP31.79.935.65.3
TCBI11.243.512.82.4
SW10.53.711.82.0
PF9.93.510.92.0
DASS-21
D4.14.23.02.7
A4.03.53.53.0
S6.24.45.62.6
M = mean value; sd = standard deviation.
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Share and Cite

MDPI and ACS Style

Ranieri, J.; Di Giacomo, D.; Guerra, F.; Cilli, E.; Martelli, A.; Ciciarelli, V.; Ventura, A.; Fargnoli, M.C. Early Diagnosis of Melanoma and Breast Cancer in Women: Influence of Body Image Perception. Int. J. Environ. Res. Public Health 2022, 19, 9264. https://doi.org/10.3390/ijerph19159264

AMA Style

Ranieri J, Di Giacomo D, Guerra F, Cilli E, Martelli A, Ciciarelli V, Ventura A, Fargnoli MC. Early Diagnosis of Melanoma and Breast Cancer in Women: Influence of Body Image Perception. International Journal of Environmental Research and Public Health. 2022; 19(15):9264. https://doi.org/10.3390/ijerph19159264

Chicago/Turabian Style

Ranieri, Jessica, Dina Di Giacomo, Federica Guerra, Eleonora Cilli, Alessandra Martelli, Valeria Ciciarelli, Alessandra Ventura, and Maria Concetta Fargnoli. 2022. "Early Diagnosis of Melanoma and Breast Cancer in Women: Influence of Body Image Perception" International Journal of Environmental Research and Public Health 19, no. 15: 9264. https://doi.org/10.3390/ijerph19159264

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop