Publications by authors named "Melanie Lyden"

Introduction: The American Association of Endocrine Surgeons drafted Entrustable Professional Activities for Comprehensive Endocrine Surgery to assess trainees in core topics.

Methods: Fourteen Entrustable Professional Activities were defined. There were 10 "core" Entrustable Professional Activities, with 6 having 3 phases (pre-, intra-, and postoperative) and 4 having a single phase.

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Oncocytic adrenal neoplasms, defined by ≥90 % of oncocytic cells, are rare. The significance of oncocytic changes within an adrenal neoplasm remains unclear. A retrospective study of adults who underwent adrenalectomy at a large center identified pure oncocytic neoplasms on final pathology (1997-2022).

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  • The study reviewed 401 patients who underwent genetic testing for familial hypocalciuric hypercalcemia, with 83% testing negative for mutations and only 11% testing positive.
  • Findings showed that patients with mutations had lower median urine calcium levels compared to non-mutated patients, but no significant difference in parathyroid hormone levels across groups.
  • The effectiveness of urine calcium measurements and calcium-to-creatinine clearance ratios in identifying familial hypocalciuric hypercalcemia was found to be poor, with areas under the curve indicating low diagnostic performance.
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Context: Data on giant pheochromocytomas (PHEO), defined based on size ≥ 10 cm, are scarce.

Objective: to compare presentation, management, and outcomes of patients with giant vs non-giant PHEOs.

Design: retrospective cohort study, 2000-2023.

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Background: Percutaneous ethanol ablation has emerged as a treatment for recurrent papillary thyroid carcinoma in the lateral neck after compartment-oriented therapeutic lymphadenectomy. However, the safety and utility of percutaneous ethanol ablation as a primary treatment modality for lateral neck metastases remains undefined. We aimed to investigate long-term outcomes of percutaneous ethanol ablation of lateral neck papillary thyroid carcinoma recurrence both with and without prior lymphadenectomy.

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Purpose: The purpose of this study is to evaluate the association between hyperparathyroidism (PHPT), parathyroid hormone levels, and calcium levels in patients diagnosed with benign fibro-osseous lesions such as fibrous dysplasia (FD), ossifying fibroma (OF), central giant cell granulomas (GCG).

Methods: This is a retrospective, single-center study from a sample of patients who underwent surgical treatment of FD, OF, and GCG at Mayo Clinic between 1996 and 2021. Patient demographics, history of PHPT, histopathological diagnosis, and relevant laboratory values such as parathyroid hormone (PTH), serum calcium, vitamin D, and alkaline phosphatase were collected.

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  • Current research indicates that cortisol-secreting adrenocortical carcinoma has a poorer prognosis compared to non-secreting types, but the impact of other secretory subtypes was unclear prior to this study.
  • The study analyzed data from 807 patients with adrenocortical carcinoma over 23 years, showing different overall survival rates based on secretory subtype, with cortisol-secreting patients having a median survival of 36 months and non-secreting patients 115 months.
  • Mixed cortisol/androgen secreting tumors were linked to worse overall survival, while the type of secretion did not significantly affect survival outcomes in patients who underwent complete resection (R0).
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Background: Protein-truncating germline pathogenic variants in the N- and C-terminal exons (2, 9, and 10) of the MEN1 gene may be associated with aggressive pancreatic neuroendocrine tumors. However, the impact of these variants on parathyroid disease is poorly understood. We sought to investigate the effects of genotype and surgical approach on clinical phenotype and postoperative outcomes in patients with multiple endocrine neoplasia type 1 (MEN1)-related primary hyperparathyroidism.

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Background: We aim to evaluate the incidence of venous thromboembolism (VTE) following adrenalectomy.

Methods: A retrospective analysis of the Collaborative Endocrine Surgery Quality Improvement Program was performed to assess incidence for VTE, including pulmonary embolism or deep vein thrombosis, in adults undergoing adrenalectomy (2014-2022).

Results: 2567 patients undergoing adrenalectomy were included.

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Introduction: Ethanol ablation can be utilized to manage insulinoma. We aimed to analyze our outcomes of endoscopic ultrasound (EUS) and intraoperative ultrasound (IOUS) guided Ethanol ablation of insulinoma.

Methods: A single institution retrospective review of adults undergoing Ethanol ablation of benign pancreatic insulinoma (2007-2022) was performed.

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Introduction: Parathyroidectomy is underperformed despite clear benefits in primary hyperparathyroidism (PHPT). We evaluated disparities in receipt of parathyroidectomy following PHPT diagnosis to explore barriers to care.

Methods: Adults diagnosed with PHPT 2013-2018 at a health system were identified.

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Introduction: Patients with primary hyperparathyroidism (1HPT) undergoing reoperative or subtotal parathyroidectomy (PTX) may undergo autotransplantation (ATX) when the viability of remaining tissue is unknown. This study aims to identify whether intraoperative parathyroid hormone levels (IOPTH) can determine ATX candidacy.

Methods: Patients with 1HPT who underwent PTX with ATX at our institution were identified.

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Background: In recent years, fluorescence imaging-relying both on parathyroid gland autofluorescence under near-infrared light and angiography using the fluorescent dye indocyanine green-has been used to reduce risk of iatrogenic parathyroid injury during thyroid and parathyroid resections, but no published guidelines exist regarding its use. In this study, orchestrated by the International Society for Fluorescence Guided Surgery, areas of consensus and nonconsensus were examined among international experts to facilitate future drafting of such guidelines.

Methods: A 2-round, online Delphi survey was conducted of 10 international experts in fluorescence imaging use during endocrine surgery, asking them to vote on 75 statements divided into 5 modules: 1 = patient preparation and contraindications to fluorescence imaging (n = 11 statements); 2 = technical logistics (n = 16); 3 = indications (n = 21); 4 = potential advantages and disadvantages of fluorescence imaging (n = 20); and 5 = training and research (n = 7).

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Article Synopsis
  • Primary Hyperparathyroidism (PHPT) is rarely found in children, and this study analyzed surgical outcomes in patients under 21 from 1994 to 2020.
  • Out of 66 patients, many were symptomatic at diagnosis, with notable familial syndromes present in a portion of cases, specifically MEN-1.
  • Results showed that sporadic cases had lower rates of recurrence compared to familial cases, highlighting the need for ongoing monitoring in patients with family histories of PHPT.
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Background: Discrimination between adrenocortical carcinoma and lipid-poor cortical adenoma preoperatively is frequently difficult as these two entities have overlapping imaging characteristics. Differentiation will allow for the selection of the most appropriate operative approach and may help prevent over-treatment. We aimed to identify imaging features that could preoperatively differentiate adrenocortical carcinoma from lipid-poor cortical adenoma and use them in a novel imaging-based score.

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Background: Focused parathyroidectomy in primary hyperparathyroidism is possible with accurate preoperative localization. A growing body of data exists regarding the role of radio-labeled C choline positron emission tomography/computed tomography. In cases of nonlocalized disease, it may be a useful adjunct to ultrasound, (123)I/(99)Tc-sestamibi (I-123 sestamibi), or 4-dimensional computed tomography imaging.

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  • Bilateral idiopathic hyperaldosteronism (IHA) accounts for 60% of primary aldosteronism cases, with medical management being the main treatment, but unilateral adrenalectomy is debated as a palliative option.* -
  • A study reviewed 24 patients who had undergone unilateral adrenalectomy for IHA, showing most had preoperative hypokalemia and required multiple antihypertensives that decreased post-surgery, with no significant complications.* -
  • The results suggest that unilateral adrenalectomy can improve blood pressure control and potassium levels in select patients with bilateral hyperaldosteronism, but more extensive studies are needed to clarify its benefits.*
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Background: There is limited long-term follow-up of patients undergoing parathyroidectomy. Recurrence is described as 4% to 10%. This study evaluated persistence and recurrence of hypercalcemia in primary hyperparathyroidism after parathyroidectomy.

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Objective: Benign adrenal cysts are rare lesions of the adrenal glands. Limited data are available to guide management. We aimed to describe the presentation and outcomes of patients with benign adrenal cysts.

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Context: Due to its rare incidence, molecular features of primary aldosteronism (PA) in young adults are largely unknown. Recently developed targeted mutational analysis identified aldosterone-driver somatic mutations in aldosterone-producing lesions, including aldosterone-producing adenomas (APAs), aldosterone-producing nodules (APNs), and aldosterone-producing micronodules, formerly known as aldosterone-producing cell clusters.

Objective: To investigate histologic and genetic characteristics of lateralized PA in young adults.

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Article Synopsis
  • The study compares characteristics and outcomes of insulinoma patients with sporadic cases versus those with Multiple Endocrine Neoplasia type 1 (MEN-1), highlighting differences in demographics, tumor features, and survival rates.
  • Results indicated that while both groups had similar rates of malignancy (around 16-18%), MEN-1 patients were diagnosed at a younger age and presented with larger benign tumors requiring surgery.
  • The findings suggest that MEN-1 patients often have multiple insulinomas and that younger patients with multifocal neuroendocrine tumors and hyperinsulinism should be screened for MEN-1 syndrome.
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Objective: Cystic adrenal mass is a rare imaging presentation of pheochromocytoma. We aimed to describe the clinical, biochemical and imaging characteristics of patients with cystic pheochromocytoma.

Design: Single-centre, retrospective study, 2000-2020.

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Background: The anatomic boundaries of lymphadenectomy for adrenocortical carcinoma (ACC) are not defined.

Methods: Adults undergoing resection of ACC were included. Locations were categorized based on positive LN locations on final pathology.

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Background: Until 2015, standard of care for low-risk papillary thyroid cancer (PTC) >1 cm was a total or near-total thyroidectomy. Despite changes in guidelines and surgical management of low-risk PTC since 2015, little data are available regarding the effect on the need for additional surgery or risk for development of lymph node metastases. Our aim was to determine outcomes in patients who underwent initial thyroid lobectomy for low-risk PTC at a high-volume tertiary care institution.

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