Idiopathic Intracranial Hypertension: Epidemiology, pathophysiology, clinical features and contemporary management.

Idiopathic Intracranial Hypertension (IIH) is a syndrome of increased intracranial pressure (ICP) without evident cause. The exact pathogenesis of IIH remains elusive but it is also plausible that the syndrome represents the common final pathway of several different mechanisms. IIH has an estimated incidence of 1-3 per 100 000 and a predilection for obese women of childbearing age.  Presentation involves symptomatology and semiology of elevated intracranial pressure with headache being the most common. Visual disturbances can be devastating, progressive and may result in permanent visual loss. Moreover, pulsatile tinnitus is frequently encountered. However, asymptomatic presentations are also not uncommon with patients diagnosed after routine ophthalmological examination illustrates papilledema. Diagnosis is based upon the Friedman’s criteria. Absence of hydrocephalus or mass lesion and normal cerebrospinal fluid (CSF) composition need to be confirmed. Several treatment modalities have been suggested, varying from non-surgical (weight loss, drugs such as acetazolamide, serial lumbar puncture) to interventional and surgical (CSF diversion procedures, optic nerve sheath fenestration (ONSF), endovascular venous sinus stenting, or even bariatric surgery). There are very few RCTs to critically assess these therapies and, consequently, no consensus on the optimal management of IIH.

Canalicular adenoma with unicystic morphology. A rare entity

Canalicular adenoma (CA) is a benign salivary gland tumor (SGT) almost exclusively affecting the minor salivary glands, predominantly of the upper lip, and exhibiting characteristic histopathologic features. As observed in several other SGTs, a commonly

A Rare Variation of Transverse Testicular Ectopia (TTE) in a Young Adult as an Incidental Finding during Investigation for Testicular Pain

Transverse testicular ectopia (TTE) with fused vas deferens is an extremely rare clinical entity. Herein, we present a case of a 19-year-old patient with persistent left testicular pain lasting for a week. Clinical examination revealed an empty right hemiscrotum, a normal left-sided descended testis, and in close proximity a mass-like structure resembling testicular parenchyma. Laboratory tests were significant for elevated follicle-stimulating hormone (FSH), while sperm count revealed azoospermia. Ultrasound imaging (US) of the scrotum demonstrated the presence of both testes in the same left hemiscrotum with varicocele and no signs of inguinal hernia. Magnetic resonance imaging (MRI) of the penis and scrotum revealed TTE with a single, fused vas deferens, and hypoplastic seminal vesicles. Surgical intervention by means of microsurgical sperm retrieval and transseptal orchidopexy were considered but not performed, primarily owing to the patient’s unwillingness and to a lesser extent due to the restriction that the short and fused vas would pose in an attempt to transpose the ectopic testis. Therefore, an annual follow-up was recommended

Plexiform Schwannoma of the Penis: A Rare Subtype of Genital Schwannoma

Schwannomas are benign, encapsulated neurogenic tumors which present in diverse histological subtypes despite the limited variety of their cellular constituents. These include the cellular, ancient, cystic, epithelioid, melanotic, psammomatous, schwannoma with pseudoglandular elements, and plexiform varieties. The plexiform schwannoma (PS) represents 4.3% of all schwannomas. These lesions are commonly encountered in the head and neck region and are extremely rare in the penis. To the best of our knowledge only 34 cases of penile schwannomas have been reported and this is the 3rd case of plexiform penile schwannoma. A 39-year-old patient presented to our andrology outpatient clinic complaining for two painful penile nodules. The lesions were located on the dorsum of the penile shaft. His medical history was insignificant for penile trauma and sexual transmitted diseases. The masses measured 2x1 cm and 0.5x1 cm. After sonographic and magnetic resonance evaluation the patient was admitted to theatre and underwent topical resection of the lesions. Histopathology revealed plexiform schwannoma. Postoperatively, penile tenderness and hyperesthesia ensued which was managed with pregabalin administration and topical corticosteroids. Plexiform schwannomas are rare in the penile region. Surgical excision is inevitably the only way to diagnose and treat the lesions. They must be differentiated by a variety of malignant and benign clinical conditions. Topical excision suffices for oncological control and allows for acceptable functional outcomes

Response of Lead Fluoride (PbF₂) Crystal under X-ray and Gamma Ray Radiation

Background: In this research, the response of a 10 × 10 × 10 mm3 commercially available PbF2 crystal was experimentally assessed under X-ray and gamma ray radiation to verify the possible application of this material in X-ray medical imaging. Methods: The measurements were performed under X-ray from 50 to 130 kVp and gamma ray excitation (Tc-99m 140 keV and I-131 365 keV). The PbF2 response was experimentally assessed by the determination of the absolute luminescence efficiency (AE), X-ray luminescence efficiency (XLE), and the stopping power of this scintillating crystal in terms of the energy absorption efficiency (EAE). The results were compared with bismuth germanate (BGO) crystal, which is commonly used in medical imaging modalities. Results: The AE of PbF2 gradually decreased from 50 kVp up to 130 kVp. The maximum value was 0.61 efficiency units (EU) at 140 keV, and the minimum value was 0.03 EU at 71 keV (130 kVp). Similarly, low values appeared for the XLE, where the maximum value was 16.9 × 10−5 at 140 keV. Conclusions: These findings show that the PbF2 scintillator has unacceptably low luminescence efficiency. Although PbF2 can effectively absorb radiation, the scintillation light, at room temperatures, is negligible, and, thus, it could not be used in medical imaging applications in the examined energy range

Dissociation between visuospatial neglect assessment tasks and its neuroanatomical substrates: a case report

Visuospatial neglect possesses significant heterogeneity in clinical features and neuroanatomical substrates. Behavioral dissociations on different neglect tasks have been reported in the past, and the investigation of their respective anatomical correlates at cortical and, to a lesser degree, subcortical levels has been attempted in stroke studies. We report a patient with a neoplasm occupying the right ventral post-central gyrus and anterior supramarginal gyrus. The patient was admitted preoperatively with dissociation on the performance of neglect tasks, showing clinical deficits in the line bisection task and clock drawing, but not on the cancelation task. The patient underwent an awake craniotomy for tumor excision. Intraoperative visuospatial mapping was employed by applying direct electrical stimulation (DES) to the supramarginal gyrus and the ventral branch of the superior longitudinal fasciculus (SLF III) during the line bisection task. According to our findings, DES was ineffective at the cortical level, but it induced strong rightward bias when applied subcortically at the SLF III. By combining our preoperative and intraoperative anatomical and clinical data, we suggest that the posterior part of the SLF III might have a distinct role in the perceptual component of neglect. Our findings are discussed within the context of previous literature supporting the notion that particular behavioral features of spatial neglect are mediated by different white-matter connections

Recurrence in Oral Premalignancy: Clinicopathologic and Immunohistochemical Analysis

Oral leukoplakia (OL) has a propensity for recurrence and malignant transformation (MT). Herein, we evaluate sociodemographic, clinical, microscopic and immunohistochemical parameters as predictive factors for OL recurrence, also comparing primary lesions (PLs) with recurrences. Thirty-three patients with OL, completely removed either by excisional biopsy or by laser ablation following incisional biopsy, were studied. Selected molecules associated with the STAT3 oncogenic pathway, including pSTAT3, Bcl-xL, survivin, cyclin D1 and Ki-67, were further analyzed. A total of 135 OL lesions, including 97 PLs and 38 recurrences, were included. Out of 97 PLs, 31 recurred at least once and none of them underwent MT, during a mean follow-up time of 48.3 months. There was no statistically significant difference among the various parameters in recurrent vs. non-recurrent PLs, although recurrence was most frequent in non-homogeneous lesions (p = 0.087) and dysplastic lesions recurred at a higher percentage compared to hyperplastic lesions (34.5% vs. 15.4%). Lower levels of Bcl-xL and survivin were identified as significant risk factors for OL recurrence. Recurrences, although smaller and more frequently homogeneous and non-dysplastic compared to their corresponding PLs, exhibited increased immunohistochemical expression of oncogenic molecules, especially pSTAT3 and Bcl-xL. Our results suggest that parameters associated with recurrence may differ from those that affect the risk of progression to malignancy and support OL management protocols favoring excision and close monitoring of all lesions