Publications by authors named "Mortini P"

Spinal cord injury (SCI) causes severe motor and sensory deficits, and there are currently no approved treatments for recovery. Nearly 70% of patients with SCI experience pathological muscle cocontraction and spasticity, accompanied by clinical signs such as patellar hyperreflexia and ankle clonus. The integration of epidural electrical stimulation (EES) of the spinal cord with rehabilitation has substantial potential to improve recovery of motor functions; however, abnormal muscle cocontraction and spasticity may limit the benefit of these interventions and hinder the effectiveness of EES in promoting functional movements.

View Article and Find Full Text PDF

TSH-secreting pituitary adenoma (TSHoma) is the rarest functioning pituitary tumor, with an increasing incidence over the last decades. Diagnosis is often delayed, exposing patients to a high risk of developing chronic complications of long-standing hyperthyroidism. Although thyroid hormone excess is a recognized cause of secondary osteoporosis, very few studies have investigated skeletal damage in patients with TSHoma, with data limited to bone turnover markers (BTM) and a study on the prevalence of radiological vertebral fractures (VFs) incidentally detected on chest X-ray, whereas data on bone mineral density (BMD) are anecdotal.

View Article and Find Full Text PDF

Glioblastoma (GBM) is the most common, fast-growing, and aggressive malignant primary CNS tumor, with a survival time of ~15 months despite the use of surgery and adjuvant treatments. In recent years, there has been a growing interest in exploring the potential contribution of hemostasis and platelet activation in GBM biology. The present study assessed the association between the pre-operative coagulation profile [as indicated by prothrombin time (PT) ratio and activated partial thromboplastin time (aPTT) ratio], overall platelets (PLT) count and the mean platelet volume (MPV) with tumoral characteristics and overall survival in patients with isocitrate dehydrogenase-wildtype (IDH-wt) GBM.

View Article and Find Full Text PDF
Article Synopsis
  • This study looked at the safety and effectiveness of a treatment called Gamma-knife stereotactic radiosurgery (SRS-GK) for a type of brain tumor called radiation-induced meningiomas (RIMs) at a hospital in Italy.
  • They included data from 13 patients and found that 26% improved, while 52% stayed the same and 22% got worse, with a good control rate over 5 years.
  • In a bigger analysis, including 146 patients, the overall success rate was high, but some patients experienced side effects like swelling, showing that while SRS-GK works well, there can be risks involved.
View Article and Find Full Text PDF

Metastatic spread to the central nervous system (CNS) is frequent in anaplastic lymphoma kinase ( ALK )-rearranged non-small cell lung cancer (NSCLC) and has an important impact on patient prognosis and quality of life. Leptomeningeal involvement may occur in up to 10% of cases of ALK-positive NSCLC. Lorlatinib is a third-generation ALK inhibitor that has excellent CNS penetrability and demonstrated its efficacy both in pretreated and treatment-naive patients.

View Article and Find Full Text PDF
Article Synopsis
  • A study focused on acromegaly patients examined if their growth hormone (GH) response to an oral glucose tolerance test (OGTT) could predict the likelihood of disease recurrence after surgery.
  • Researchers found that a paradoxical GH response occurred in about 34% of the studied patients and was linked to a significantly lower recurrence rate of acromegaly (3.4%) compared to those with a non-paradoxical response (12.0%).
  • The findings suggest that GH responsiveness to OGTT can help forecast the long-term outcomes for acromegaly patients following surgical treatment.
View Article and Find Full Text PDF
Article Synopsis
  • Stereotactic radiosurgery (SRS) has become an important treatment for acromegaly, especially for managing growth hormone-secreting pituitary adenomas.
  • A systematic review and meta-analysis of 27 studies revealed an endocrine remission rate of 40% to 60%, with overall estimates of 46% for remission and 48% for 5-year remission probabilities after SRS.
  • The analysis also found that new hypopituitarism occurred in 23% of cases, and the incidence of radiation-induced optic neuropathy was low, ranging from 0% to 6%.
View Article and Find Full Text PDF

Purpose: Vertebral fractures (VFs), the hallmark of skeletal fragility, have been reported as an emerging complication in patients with pituitary diseases associated with hormonal excess and/or deficiency, independently from bone mineral density. Non-functioning pituitary adenoma (NFPA) is amongst the most frequent pituitary adenomas; however, skeletal health in this context has never been investigated. We aimed at assessing the prevalence and the determinants of morphometric VFs in patients with NFPA.

View Article and Find Full Text PDF

Background: Papillary craniopharyngiomas harbor the BRAF V600E mutation, which paves the way for using BRAF inhibitor molecules to treat tumors refractory to standard therapies. Single case reports confirmed the efficacy of targeted therapy. However, most reports were limited by the short follow-up.

View Article and Find Full Text PDF

Background And Objectives: The retrosigmoid approach with transtentorial extension (RTA) allows us to address posterior cranial fossa pathologies that extend through the tentorium into the supratentorial space. Incision of the tentorium cerebelli is challenging, especially for the risk of injury of the cranial nerve (CN) IV. We describe a tentorial incision technique and relevant anatomic landmarks.

View Article and Find Full Text PDF

Background And Purpose: Early brain injury is a major determinant of clinical outcome in poor-grade (World Federation of Neurosurgical Societies [WFNS] IV-V) aneurysmal SAH and is radiologically defined by global cerebral edema. Little is known, though, about the effect of global intracranial hemorrhage volume on early brain injury development and clinical outcome.

Materials And Methods: Data from the multicentric prospective Poor-Grade Aneurysmal Subarachnoid Hemorrhage (POGASH) Registry of consecutive patients with poor-grade aneurysmal SAH admitted from January 1, 2015, to August 31, 2022, was retrospectively evaluated.

View Article and Find Full Text PDF

Background And Objectives: Gamma Knife radiosurgery (GKRS), typically administered in a single session (S-GKRS), is an effective treatment for nonfunctioning pituitary adenoma (NFPA). For lesions close to the optic pathway, the use of hypofractionated radiosurgery is growing. This study seeks to compare the results of S-GKRS vs fractionated-GKRS (F-GKRS) for NFPAs adjacent to the optic pathway.

View Article and Find Full Text PDF

Central neurocytomas (CN) are rare tumors within the central nervous system. Originating from the septum pellucidum and subependymal cells, they are typically found in the third and lateral ventricles. For this reason, they may lead to hydrocephalus and increased intracranial pressure.

View Article and Find Full Text PDF

Purpose: Thyrotropin (TSH)-secreting pituitary adenoma (TSHoma) is a rare cause of TSH-dependent hyperthyroidism. The first therapeutic option is surgery. Medical treatment with somatostatin analogs is also effective.

View Article and Find Full Text PDF

Objective: First-line prolactin-secreting tumor (PST) management typically involves treatment with dopamine agonists and the role of surgery remains to be further explored. We examined the international experience of 12 neurosurgical centers to assess the patient characteristics, safety profile, and effectiveness of surgery for PST management.

Methods: Patients surgically treated for PST from January 2017 through December 2020 were evaluated for surgical characteristics, outcomes, and safety.

View Article and Find Full Text PDF

Purpose: The 14th Acromegaly Consensus Conference was convened to consider biochemical criteria for acromegaly diagnosis and evaluation of therapeutic efficacy.

Methods: Fifty-six acromegaly experts from 16 countries reviewed and discussed current evidence focused on biochemical assays; criteria for diagnosis and the role of imaging, pathology, and clinical assessments; consequences of diagnostic delay; criteria for remission and recommendations for follow up; and the value of assessment and monitoring in defining disease progression, selecting appropriate treatments, and maximizing patient outcomes.

Results: In a patient with typical acromegaly features, insulin-like growth factor (IGF)-I > 1.

View Article and Find Full Text PDF
Article Synopsis
  • - Extraskeletal chondromas (EC) are rare, benign tumors mainly found in the upper and lower extremities, with only four previous pediatric cases reported in the neck's anterior compartment, and this text discusses the first case in the posterior compartment.
  • - Diagnosis of EC can be challenging as they may be mistaken for malignant tumors on imaging, highlighting the need for thorough diagnostic procedures prior to surgery.
  • - The treatment primarily involves surgical excision, which shows promising results, as demonstrated by symptom improvement and no recurrence in the presented case after six months of follow-up.
View Article and Find Full Text PDF

Background: Crooke cell adenomas (CCAs) are a rare, aggressive subset of secretory pituitary corticotroph adenomas (sCTAs) found in 5%-10% of patients with Cushing disease. Multiple studies support worse outcomes in CCAs but are limited by small sample size and single-institution databases. We compared outcomes in CCA and sCTA using a multicenter, international retrospective database of high-volume skull base centers.

View Article and Find Full Text PDF

Pineal region tumors (PTs) represent extremely rare pathologies, characterized by highly heterogeneous histological patterns. Most of the available evidence for Gamma Knife radiosurgical (GKSR) treatment of PTs arises from multimodal regimens, including GKSR as an adjuvant modality or as a salvage treatment at recurrence. We aimed to gather existing evidence on the topic and analyze single-patient-level data to address the efficacy and safety of primary GKSR.

View Article and Find Full Text PDF

Importance: Benchmarks aid in improve outcomes for surgical procedures. However, best achievable results that have been validated internationally for transsphenoidal surgery (TS) are not available.

Objective: We aimed to establish standardized outcome benchmarks for TS of pituitary adenomas.

View Article and Find Full Text PDF
Article Synopsis
  • The text discusses various medical conditions affecting the brain and spinal cord, previously grouped under terms like Phacomatosis and genodermatosis, which are now outdated.
  • With advancements in genetics, particularly whole-genome sequencing, researchers are identifying new cancer susceptibility genes, revealing complexities in tumor syndromes caused by mutations in different or the same genes.
  • The chapter highlights common central nervous system syndromes, including neurofibromatosis types 1 and 2, von Hippel-Lindau disease, and tuberous sclerosis complex, along with syndromes with more external symptoms like Cowden and Li-Fraumeni syndromes, and anticipates future targeted therapies.
View Article and Find Full Text PDF

The presented tumors in this chapter are somewhat very rare, and their management is still debated due to the scarcity of information about their cell of origin, behavior, and biology. Treatment options are still limited, but we are confident that in the near future by discovering the genetic and biological mechanisms that drive tumor growth we will be able to offer new target therapies that should be flanked by surgery, radiotherapy, and chemotherapeutic agents actually in use. The purpose of this chapter is to highlight the most important known characteristics of these tumors offering the chance to recognize the disease and then offer the best opportunity for treatment to patients.

View Article and Find Full Text PDF
Article Synopsis
  • Brain tumors and orbital tumors are diverse in type, with varying characteristics and treatment approaches, where dermoid cysts and cavernous hemangiomas are common benign types and non-Hodgkin lymphoma is the leading malignant tumor.
  • Clinical symptoms of orbital lesions can overlap, making accurate diagnosis essential, and imaging studies play a crucial role in differentiating between types and planning treatment.
  • Surgical intervention is the preferred treatment for most orbital lesions, but depending on the tumor's nature and extent, chemotherapy and radiotherapy may also be necessary in some cases.
View Article and Find Full Text PDF