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1.
Ned Tijdschr Geneeskd ; 1662022 10 24.
Article in Dutch | MEDLINE | ID: mdl-36300473

ABSTRACT

BACKGROUND: The vulvar form of lymphangioma circumscriptumis a rare condition. It is part of the acquired lymphangiectasia and arises secondary, for example, after surgery, radiotherapy for malignancies in the pelvic region, inflammation in which vulvar lymphedema occurs or Morbus Crohn. CASE DESCRIPTION: A 44-year-old woman presented to the gynaecology outpatient department with a vulvar abnormality that was accompanied by pain and pruritus. Her medical history consisted of premalignant cervical abnormalities and a vulvar lichen simplex chronicus. A biopsy was taken and the diagnosis lymphangioma circumscriptum was made. Due to the growth and the complaints, the decision was made to remove the lesion in the operating room. CONCLUSION: Lymphangioma circumscriptum is a rare condition that is often misdiagnosed. This case may describe the development of lymphangioma circumscriptum from a lichen simplex chronicus, which has not been described before. It also demonstrates that surgical treatment appears to be a good treatment with few complications in the postoperative course.


Subject(s)
Lymphangioma , Neurodermatitis , Vulvar Diseases , Vulvar Neoplasms , Female , Humans , Adult , Vulvar Neoplasms/diagnosis , Vulvar Neoplasms/surgery , Neurodermatitis/complications , Neurodermatitis/pathology , Lymphangioma/diagnosis , Lymphangioma/surgery , Vulva/pathology , Vulvar Diseases/etiology , Rare Diseases
2.
Gynecol Oncol ; 162(2): 360-367, 2021 08.
Article in English | MEDLINE | ID: mdl-34112514

ABSTRACT

OBJECTIVE: To determine the predictive value of lumbar skeletal muscle mass and density for postoperative outcomes in older women with advanced stage ovarian cancer. METHODS: A multicenter, retrospective cohort study was performed in women ≥ 70 years old receiving surgery for primary, advanced stage ovarian cancer. Skeletal muscle mass and density were assessed in axial CT slices on level L3. Low skeletal muscle mass was defined as skeletal muscle index < 38.50 cm2/m2. Low skeletal muscle density was defined as one standard deviation below the mean (muscle attenuation < 22.55 Hounsfield Units). The primary outcome was any postoperative complication ≤ 30 days after surgery. Secondary outcomes included severe complications, infections, delirium, prolonged hospital stay, discharge destination, discontinuation of adjuvant chemotherapy and mortality. RESULTS: In analysis of 213 patients, preoperative low skeletal muscle density was associated with postoperative complications ≤ 30 days after surgery (Odds Ratio (OR) 2.83; 95% Confidence Interval (CI) 1.41-5.67), severe complications (OR 3.01; 95%CI 1.09-8.33), infectious complications (OR 2.79; 95%CI 1.30-5.99) and discharge to a care facility (OR 3.04; 95%CI 1.16-7.93). Preoperative low skeletal muscle mass was only associated with infectious complications (OR 2.32; 95%CI 1.09-4.92). In a multivariable model, low skeletal muscle density was of added predictive value for postoperative complications (OR 2.57; 95%CI 1.21-5.45) to the strongest existing predictor functional impairment (KATZ-ADL ≥ 2). CONCLUSION: Low skeletal muscle density, as a proxy of muscle quality, is associated with poor postoperative outcomes in older patients with advanced stage ovarian cancer. These findings can contribute to postoperative risk assessment and clinical decision making.


Subject(s)
Cytoreduction Surgical Procedures/adverse effects , Ovarian Neoplasms/surgery , Postoperative Complications/epidemiology , Sarcopenia/epidemiology , Aged , Aged, 80 and over , Female , Humans , Length of Stay , Muscle, Skeletal/diagnostic imaging , Neoplasm Staging , Ovarian Neoplasms/complications , Ovarian Neoplasms/diagnosis , Postoperative Complications/etiology , Preoperative Period , Retrospective Studies , Risk Assessment/statistics & numerical data , Risk Factors , Sarcopenia/diagnosis , Sarcopenia/etiology , Tomography, X-Ray Computed/statistics & numerical data
3.
Cancer Epidemiol Biomarkers Prev ; 30(4): 743-750, 2021 04.
Article in English | MEDLINE | ID: mdl-33563645

ABSTRACT

BACKGROUND: Atypical glandular cells (AGC) are rare abnormalities found on cervical cytology associated with a range of lesions of the female reproductive system. We compared the risk of cervical and other gynecologic cancers following AGC on cervical cytology with the risk following squamous cell abnormalities of comparable severity. METHODS: We used data from the Dutch Pathology Archive (PALGA) from 2000 to 2015 to categorize cervical cytology tests into groups based on most severe cytologic abnormality and correlated follow-up advice (normal cytology and "no follow-up" advice, squamous-cell-based, AGC-based, and combined AGC/squamous-cell based each with either repeat testing or referral advice). Cancer data were linked from the Netherlands Cancer Registry. Cox proportional hazard models were calculated stratified by age [younger (<50 years) and older (50+ years)], adjusted for number of previous primary cytology tests. RESULTS: 8,537,385 cytology smears and 9,061 cancers were included. When repeat cytology testing was advised, HRs of cervical cancer (younger women: HR, 6.91; 95% CI, 5.48-8.71; older women: HR, 3.98; 95% CI, 2.38-6.66) or other gynecologic cancer diagnosis in younger women (HR, 2.82; 95% CI, 1.39-5.74) were significantly higher after an AGC-based abnormality compared with squamous-based abnormalities. Hazards were also significantly higher for "referral" advice cytology, except for cervical cancer among older women (HR, 0.88; 95% CI, 0.63-1.21). CONCLUSIONS: AGC indicates an increased risk of gynecologic cancer compared with squamous-based abnormalities of comparable severity. IMPACT: Gynecologists should be alert for cervical and endometrial cancers when examining women referred following AGC.


Subject(s)
Atypical Squamous Cells of the Cervix/pathology , Genital Neoplasms, Female/pathology , Adult , Female , Humans , Middle Aged , Neoplasm Grading , Netherlands , Papanicolaou Test , Registries , Retrospective Studies , Risk , Uterine Cervical Neoplasms/pathology
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