ACTA ENDOCRINOLOGICA (BUC)

The International Journal of Romanian Society of Endocrinology / Registered in 1938

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Year Volume Issue First page
10.4183/aeb.
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  • Perspectives

    Lazarus JH, Taylor PN

    Hypothyroxinaemia and Brain Development

    Acta Endo (Buc) 2016 12(1): 1-6 doi: 10.4183/aeb.2016.1

    Abstract
    The aim of this review is to indicate the current position on the role of thyroxine (T4) and fetal brain development with particular relevance to the human situation. Adequate maternal iodine nutrition and maternal circulating thyroxine (T4) concentrations are essential to ensure optimum T4 placental passage which in turn will ensure transport of T4 into fetal brain cells. These processes are discussed and the role of thyroid hormone transporters is considered. The emphasis on isolated maternal hypothyroxinaemia (IH) as an important factor affecting brain development is discussed from the animal experimental point of view as well as in the clinical setting. There is evidence of neurocognitive impairment as assessed by different modalities in children up to the age of 8 years and some suggestion of increased psychiatric disorder in older persons whose mothers had IH during gestation. Although international guidelines have not in general recommended thyroxine therapy for IH the recent demonstration of adverse obstetric outcomes in women with isolated maternal hypothyroxinaemia may warrant a revision of this strategy.
  • Case Report

    Gluhovschi G, Velciov S, Lazar E, Potencz E, Puscasiu T, Trandafirescu V, Petrica L, Bozdog G, Gluhovschi C, Bob F, Gadalean F, Lazar D

    Retroperitoneal fibrosis with favorable evolution under treatment with tamoxifen

    Acta Endo (Buc) 2010 6(1): 95-102 doi: 10.4183/aeb.2010.95

    Abstract
    Retroperitoneal fibrosis (RPF), a disease with a severe outcome due to the complications it causes, can be associated with the processes of atherosclerosis with a massive and extensive fibrosis. In this paper we present a patient with retroperitoneal fibrosis in which we noticed estrogen receptors at the level of the periaortic fibrous tissue\r\nand we obtained a regression of this process under treatment with tamoxifen.
  • Case Report

    Kozma A, Radoi V, Ursu R, Bohaltea CL, Lazarescu H, Carniciu S

    Gestational Diabetes Mellitus and the Development of Cleft Lip / Palate in Newborns

    Acta Endo (Buc) 2019 15(1): 118-122 doi: 10.4183/aeb.2019.118

    Abstract
    Background. Several studies observed metabolic disorders in pregnancy as risk factors for birth defects, including orofacial clefts. Diabetes is associated with approx. 10% of the pregnancies, but in Romania, less than 5%. An obese and diabetic woman has 3 times more risk for an offspring with a craniofacial defect than healthy women suggesting that diabetes mellitus contributes to their pathogenesis with complex mechanisms. Case report. We present the case of a newborn 4 days old, male with neonatal hypoglycemia, cleft lip and proportionate (symmetric) macrosomia. His mother is a 35 years old Caucasian woman with no important personal risk factors and no known history of diabetes mellitus. The glucose tolerance test performed to the mother at about 10 weeks during pregnancy led to the diagnosis of gestational diabetes. Discussion. The gestational diabetes mellitus diagnosed since the 10th week of pregnancy, the hyperglycemia status during pregnancy and the fetal overgrowth (macrosomia at birth) indicate the possible factors that lead to the Orofacial cleft (OFC). Conclusion. With the increased prevalence of obesity, diabetes, and the evidence of association of these syndromes with OFCs, it is recommended that mothers planning to become pregnant to follow healthy habits, maintain healthy weight, and be screened for possible diabetes prior to conception and early in pregnancy.
  • Actualities in medicine

    Tovkai OA, Palamarchuk VO, Shidlovskyi OV, Shidlovskyi VO, Kuts VV, Smoliar VA, Sheremet MI, Levchuk RD, Morozovych II, Cretoiu D, Lazaruk OV

    Rationale for the Application of Calcitonin Level in the Early Postoperative Period to Evaluate the Effectiveness of Surgical Treatment of Medullary Thyroid Cancer

    Acta Endo (Buc) 2023 19(1): 142-146 doi: 10.4183/aeb.2023.142

    Abstract
    Purpose. To determine the effectiveness of the basal calcitonin (CTb) determination in the early postoperative period to predict the possible recurrence (persistence) of medullary thyroid cancer (MTC). Material and Methods. A retrospective study of the treatment results in 194 patients with MTC (148 (76.3%) primary – group 1 and 46 (23.8%) recurrent – group 2) according to the levels of CTb in the first week after surgery and one year later. All groups were analyzed by staging, the level of preoperative and postoperative basal calcitonin 5 days and 1 year after the primary surgery. Findings. Among all patients, women prevailed – 144 (74.2%), the average age was (48.7±15.2), the average follow-up period was 67.5 months. Basal calcitonin was studied in patients of all groups in the preoperative and serially in the postoperative periods: 5 days and 1 year after the most radical surgical volumes. To test the hypothesis about the possibility of using CTb indicators in the early postoperative period, the degree of compliance with normal calcitonin indicators (≤18 pg/mL) was assessed by observation groups 5 days and 1 year after surgery. Conclusions. 1. The CTb value 5 days after surgery is no less a reliable marker of the result of surgical treatment of MTC than the currently recommended CTb measurement 2-3 months after surgery. 2. The technique is applicable for both primary and reoperations used for recurrent forms of medullary thyroid cancer.
  • General Endocrinology

    Rosianu A, Lazar E, Raica M

    Oncoprotein c-erb B2 - prognostic significance in invasive breast cancer

    Acta Endo (Buc) 2005 1(2): 145-156 doi: 10.4183/aeb.2005.145

    Abstract References
    Objective: The invasive mammary cancer is the most frequent malignant tumor of a woman. Among the potential prognostic factors are included the biomarkers which measure or are associated with biological processes involved in the tumoral progression.We studied the prognostic importance of the oncoprotein c-erbB2 in the invasive mammary cancer.\r\nMaterials and methods: We included in the study 56 female patients suffering from invasive mammary cancer.The tissue fragments were fitted in formol, included to paraffin, commonly stained with hematoxylin-eosine (HE); for the determination of the c-erbB2 we\r\nused the immunohistochemical method of the avidin-biotin (ABC) complex.\r\nResults: From the total of 56 tumors, 38 (67.9%) presented different degrees of positivity; 18 (32.1%) did not express the oncoprotein c-erbB2.\r\nConclusions: The positivity of oncoprotein c-erbB2 was correlated with the size of the tumor; the carcinomas which are not infiltrative ductal, known as having a better prognostic, were c-erbB2 negative.
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    2. Guerin M, Gabillot M, Mathieu MC et al. Structure and expression of c-erbB2 and EGFR receptor genes in inflammatory and non-inflammatory breast cancer: prognostic significance. Int. J. Cancer 1989; 43: 201. [CrossRef]
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    5. Paul P, Rosen MD, Martin L, Lesser Ph D, Crispinita D, Arrayo CLS et al.: Immunohistochemical detection of HER2/neu in patients with axillary lymph nodes negative breast carcinoma. Cancer 1995; 75(6):1320-1325. [CrossRef]
    6. Seshardi R, Firgaira FA, Horsfall DJ, Mc Caul K, Setur V, Vithen P. Clinical significance of HER2/neu oncogene amplificator in primary breast cancer. J. Clin. Oncol. 1993;11:1936-1946.
    7. Toikkanen S, Kujari H. Pure and mixed mucinous carcinomas of the breast: a clinicopathologic analysis of 61 cases with long term follow-up. Hum. Pathol. 1989;20:758-764. [CrossRef]
    8. Garcia I, Dietrich P, Aapro M, Vauthier G, Vadus L, and Engel E. Genetic alteration of c-myc, c-erbB2 and c-Ha-ras protooncogenes and clinical associations in human breast carcinomas. Cancer Res. 1989; 49:6675.
    9. Parkes HC, Lillycrop K, Howell A and Craig RK. c-erbB2 mRNA expression in human breast tumors: comparison with c-erbB2 DNA amplification and correlation with prognosis. Br. J. Cancer 1990;61: 39. [CrossRef]
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    11. Silverberg G. Steven. Principles and practice of surgical pathology, vol I, 1983: 245, 266-267, 270- 295.
    12. Rosen PP, Martin L, Crispinita L, Arrayo D, Cranor M, Borgen P, Norton L. p53 in node negative breast carcinoma: an immunohistochemical study of epidemiologic risk factors, histologic features and prognosis. HJ. Clin Oncol. 1995; 13(4): 821-830.
    13. Slamon DJ, Godolphin W, Jones LA et al. Studies of the HER2/neu proto-oncogene in human breast and ovarian cancer. Science 1989; 244:707. [CrossRef]
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    15. Wright C, Angus B, Nicholson S et al: Expression of c-erbB2 oncoprotein: a prognostic indicator in human breast cancer. Cancer Res. 1989; 49: 2087-2090.
    16. Lovekin C, Ellis JO, Lockr A et al. c-erbB2 oncoprotein expression in primary and advanced breast cancer. Br. J. Cancer 1991; 63:439. [CrossRef]
    17. Borg A, Tandon AK, Sigurdsson H et al. HER2/neu amplificattion predicts poor survival in nodepositive breast cancer. Cancer Res. 1990; 50:4332.
    18. Gasparini G, Dal Fior S, Pozza P, Bevilaqua P. Correlation of growth fraction by Ki-67 immunohistochemistry with histologic factors and hormone receptors in operable breast carcinoma. Breast Cancer Res. Treat. 1989; 14: 329-336. [CrossRef]
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  • Endocrine Care

    Cozma I, Cozma LS, Boyce RL, Ludgate ME, Lazarus JH, Lane CM

    Variation in thyroid status in patients with Graves' orbitopathy

    Acta Endo (Buc) 2009 5(2): 191-198 doi: 10.4183/aeb.2009.191

    Abstract
    Graves’ orbitopathy usually occurs in thyrotoxic patients at the presentation of the\r\nhyperthyroidism.\r\nAim: we conducted a cross sectional study over 8 and a half years of the relation\r\nbetween Graves’ orbitopathy and thyroid status in patients presenting to our joint thyroidophthalmology\r\nclinic at University Hospital of Wales.\r\nMethods: Patients with active orbitopathy were diagnosed clinically and with\r\nappropriate imaging where necessary. This series excluded patients previously treated with\r\nradioiodine or surgery for Graves’ disease. Of 259 patients 140 (54%) had not had 131I or\r\nsurgical therapy. Thirty four percent of the 140 had never been hyperthyroid of whom 19\r\n(13.5%) were euthyroid. Twenty nine of the 140 (20.7%) were hypothyroid receiving\r\nlevothyroxine at referral. There were no significant differences between the hyperthyroid\r\nand non hyperthyroid groups in the incidence of cigarette smoking, family history of thyroid\r\ndisease or maximum proptosis at presentation.\r\nResults: We found a higher prevalence of smokers than reported in the literature in\r\nmoderate and severe TAO across all thyroid status groups including hypothyroid only\r\npatients. This study has emphasized the occurrence of Graves’ orbitopathy in hypothyroid\r\npatients as well as euthyroid individuals.
  • Endocrine Care

    Fica SV, Lazar A, Albu A, Barbu C, Grigorescu M

    The impact of hyperthyroidism on glycemic control in patients with diabetes mellitus

    Acta Endo (Buc) 2006 2(2): 203-212 doi: 10.4183/aeb.2006.203

    Abstract
    Aim: to evaluate the impact of hyperthyroidism on glycemic control among patients with diabetes mellitus (DM).\r\nResearch design and methods: This retrospective study included patients with hyperthyroidism and DM admitted in Endocrinology, Nutrition Diseases and Diabetes Department of Elias University Emergency Hospital. We evaluated 37 patients (35 women/ 2 men), with a mean age of 54.7?15.3 years and duration of diabetes 8.1?7.49 years; 20 patients with Graves diseases (54%), 10 with toxic multinodular goiter (27%), 5 with autonomous hyperfunctioning adenoma (13%) and 2 with amiodarone induced hyperthyroidism (5.4%). Clinical data were recorded for all our patients, as well as thyroid ultrasound exploration, laboratory analyses (glycosylated hemoglobin, free thyroxine FT4, triiodothyronine T3, thyroid stimulating hormone TSH).\r\nResults: Diabetes control was achieved with: insulin in 23 (62%) patients, antidiabetic oral agents in 9 (24%) and solely diet in 5 patients (13.5%). Hyperthyroid patients had a mean value of glycosylated hemoglobin of 9.3%?2.4% (poor glycemic control) versus 7.2%?1.6% after the treatment of hyperthyroidism. Among insulin-treated patients, the average need of insulin in hyperthyroid status was 0.72 u/kg versus 0.55 u/kg when the patients became euthyroid (p<0.01). We found a significant association between type 1 diabetes mellitus and Graves&#8217; disease compared to toxic multinodular goiter (80% vs 50%, p<0.01).\r\nConclusions: The presence of hyperthyroidism aggravates glycemic control of the patients with diabetes mellitus and increases insulin need in insulin-treated patients. Once the thyroid function was stable, the insulin need decreased significantly (p<0.01). Hyperthyroidism should be radically treated to obtain a good glycemic control. Type 1 diabetes is significantly associated to Graves&#8217;s disease by an autoimmune mechanism.
  • Endocrine Care

    Nanu M, Ardeleanu IS, Brezan F, Nanu I, Apostol A, Moldovanu F, Lazarescu H, Gheorghiu ML, Kozma A

    Neonatal Screening for Congenital Hypothyroidism in Romania: Data From Medilog Medical Information Registry

    Acta Endo (Buc) 2019 15(2): 209-214 doi: 10.4183/aeb.2019.209

    Abstract
    Objective. Congenital hypothyroidism (CH) is one of the common preventable causes of intellectual disability in neonates, by early detection through neonatal screening. We present the 8-year experience of the National Institute for Mother and Child Health (INSMC) in using MEDILOG national registry for the neonatal screening of CH. Methods. Neonatal screening for CH, done by TSH measurement in dried blood spot, is organized in 5 regional centers, each with a reference laboratory. Results. In 2018 80% of all the newborns, from 80% of the maternity hospitals, were registered in MEDILOG. After re-testing of TSH and T4/FT4 from venous blood in positive cases, the incidence of confirmed CH in 2018 was 1/3576 - 1/ 4746. In INSMC center (which includes 26 counties and Bucharest, out of 41 counties), in 2018 the incidence of positive CH cases at screening was 1/2094 (TSH cut-off ≥17 mIU/L) and of confirmed CH cases 1/3576 newborns. For positive screening cases, the median duration from birth to the INSMC laboratory result was 19 days: median of 9 days between screening and laboratory registration and 6 days between registration and test result. Conclusion. MEDILOG registry is a practical instrument for monitoring the steps of neonatal CH screening, the incidence of CH, the evolution of the diagnosed cases, for evaluation of iodine deficiency (by neonatal TSH), and also for research, with the aim of improving early disease detection and treatment.
  • Endocrine Care

    Gussi I, Ursuleanu A, Ceausu I, Dutescu C, Lazar V, Mirciulescu C

    Longer Duration and Lower Fatal Risk of Late-onset Pregnancy-related Ovarian Hyperstimulation Syndrome

    Acta Endo (Buc) 2011 7(3): 357-363 doi: 10.4183/aeb.2011.357

    Abstract
    Background. Ovarian hyperstimulation syndrome (OHSS) is a potentially life-threatening complication of the luteal\r\nphase or early pregnancy after ovulation induction or ovarian stimulation. The late OHSS form presents an onset more than 10 days after ovulation triggering and is\r\ninfluenced by pregnancy-related HCG secretion.\r\nReport. This paper presents three cases of pregnancy-related OHSS after IVF/ICSI cycles discussing risk factors and management according to European Guidelines.\r\nResults. Individual risk factors are identified such as low BMI, high antral follicle count at the beginning of the ovarian stimulation, high estradiol over 3000 pg/ml.\r\nPatients had moderate OHSS (case 2) and severe OHSS (case 1 and 3). In-patient treatment was 3-14 days. OHSS resolved in\r\nall cases, without manifestations of the critical form.\r\nConclusion. The duration of OHSS is longer in the late form, is pregnancy-related and should be monitored for adverse\r\npregnancy outcomes. However the incidence of fatal risks is low and the treatment is successful.
  • Case Report

    Benea SN, Lazar M, Hristea A, Hrisca RM, Niculae CM, Moroti RV

    Central Hypothyroidism in Severe Sepsis

    Acta Endo (Buc) 2019 15(3): 372-377 doi: 10.4183/aeb.2019.372

    Abstract
    Objective. A partial or complete deficiency of hormone secretion by pituitary gland (hypopituitarism) is commonly seen after a pituitary apoplexy caused by an infarction of a pituitary adenoma or pituitary hyperplasia (as in Sheehan’s syndrome). Hypopituitarism may also follow surgery, when hypovolemia, anticoagulation, fat/ air/bone marrow microemboli can provoke a pituitary infarction/hemorrhage. Other causes of abrupt hypophyseal hypoperfusion, as hypovolemia during a septic shock, could also contribute. In the last mentioned situation, due to the complex endocrine-immune interrelation, sepsis could be masked and improperly managed. Case report. We report a case of a 72 years-old Caucasian woman, previously healthy, who underwent an orthopedic surgery for a femoral fracture. This event apparently triggered a central-origin hypothyroidism, misinterpreted as “post-surgical psychosis”, which, in turn, masked a symptomatology of a subsequent severe sepsis. The patient was admitted in the infectious diseases department with a severe gut-origin sepsis, needing surgery and long course antibiotics. The pituitary insufficiency was reversed. Conclusion. Pituitary apoplexy is an uncommon but potentially life-threatening disease, and could be precipitated by successive events – in our case an orthopedic surgery and a subsequent severe sepsis. It needs recognizing (has intrinsic severity and could mask other serious conditions), treat and monitor (could progress and/or reverse).