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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Title
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  • Case Report

    Kim SH, Park JH

    Adrenal Incidentaloma, Breast Cancer and Unrecognized Multiple Endocrine Neoplasia Type 1

    Acta Endo (Buc) 2019 15(4): 513-517 doi: 10.4183/aeb.2019.513

    Abstract
    Background. The incidence of adrenal incidentaloma has been increasing proportional to the use of radiologic examination. Multiple endocrine neoplasia1 (MEN1) syndrome may present with various tumors. The present study reports a case of adrenal incidentaloma with unrecognised MEN1 syndrome associated with breast cancer. Clinical case. A 48-year-old woman presented with a 2.4cm left adrenal incidentaloma on abdominal computed tomography. Her history revealed primary amenorrhea, recurrent peptic ulcer and nephrolithiasis. Laboratory and radiologic examination revealed two pancreatic tail mass lesions with markedly elevated gastrin levels (1462 pg/mL), hypercalcemia with increased parathyroid hormone levels (72 pg/mL), a 1.5cm pituitary mass with hyperprolactinemia (234 ng/mL), a 1.0cm meningioma and a nonfunctional left adrenal mass. During this image work up, a 0.6cm nodule in the right breast was incidentally detected. Surgeries (laparoscopic distal pancreatectomy, parathyroidectomy and wide local excision of breast) and pathologic findings confirmed pancreatic neuroendocrine tumors, parathyroid gland hyperplasia, and breast cancer. Carbergoline treatment for 12 months decreased prolactin levels to 27 ng/mL. Genetic testing using peripheral blood revealed a pathogenic variant in MEN1 on chr11q13 (NM_000244.3:c.1365+1_1365+11 del, GTGAGGGACAG, heterozygous). Conclusion. Considering the increasing incidence of adrenal incidentaloma and 20% prevalence of adrenal tumors in patients with MEN1, it is important to rule out MEN1 association in patients with adrenal incidentaloma. Additionally, breast cancer was detected during MEN1 workup in this case. Female patients with MEN1 are at increased risk for breast cancer. Therefore, intensified breast cancer screening at a relatively young age should be considered in female MEN1 patients.
  • Notes & Comments

    Hekimsoy Z, Eniseler EB, Erdem N, Ozdemir N

    Catamenial Diabetic Ketoacidosis

    Acta Endo (Buc) 2022 18(4): 538-540 doi: 10.4183/aeb.2022.538

    Abstract
    Diabetic ketoacidosis (DKA) is a common medical emergency situation. In rare cases, glycemic changes associated with the menstrual cycle may create a predisposing factor for DKA. In the absence of facilitating factors that may cause DKA, catamenial DKA should be considered. In the patients with catamenial DKA, increasing the insulin dose 1-2 days before menstruation may prevent the development of hyperglycemia or DKA associated with menstrual cycle. In this study, we present a 21-year-old female with type 1 diabetes mellitus (DM) that recurrently applied to our hospital due to DKA a few days prior to menstrual bleeding.
  • Actualities in medicine

    Radoi VE, Pop LG, Maioru OV, Dan A, Riza M, Novac MA, Sabau D, Kim JH, Song YJ, Bohiltea LC

    Cutting Edge Trio-WGS in Rare Genetic Syndrome Diagnosis

    Acta Endo (Buc) 2022 18(4): 541-544 doi: 10.4183/aeb.2022.541

  • Case Report

    Rha SY, Ju SH, Shin MY, Kim JM, Joung KH, Ko YH, Kim Hj, Ku BJ

    Bilateral Adrenal Lymphoma Presenting as Primary Adrenal Insufficiency

    Acta Endo (Buc) 2014 10(4): 693-698 doi: 10.4183/aeb.2014.693

    Abstract
    The incidence of primary adrenocortical insufficiency is 4.7 to 6.2 per one million. Among primary cancers developed in the adrenal gland, malignant lymphoma is very rare. We report here on an 82-year-old male patient who had primary adrenocortical insufficiency caused by bilateral adrenal lymphoma.