Subject(s)
COVID-19 , Herpesviridae Infections , Herpesvirus 8, Human , Sarcoma, Kaposi , Humans , Microscopy, Electron , SARS-CoV-2ABSTRACT
Pituitary apoplexy is a rare endocrine emergency that occurs in a small number of patients with a pituitary tumor. It is a clinical syndrome characterized by the sudden onset of headache, nausea, vomiting, visual impairment, and decreased consciousness, caused by hemorrhage and/or infarction of the pituitary gland. Pituitary apoplexy has very rarely been described during pregnancy, when it is potentially life-threatening to both the mother and the fetus, if unrecognized. Only a few cases have been published to date. The review of the existing literature underlines that pituitary apoplexy, although rare, should be borne in mind when a pregnant woman presents with severe headache and visual defects of sudden onset. After initial management, which includes intravenous glucocorticoid therapy, fluid and electrolyte replacement, the final selection of medical or surgical treatment should result from a multidisciplinary approach involving expert specialists, keeping into account both severity of clinical presentation and gestational week.
Subject(s)
Headache , Pituitary Apoplexy , Pregnancy Complications , Female , Headache/diagnosis , Headache/etiology , Headache/therapy , Humans , Pituitary Apoplexy/complications , Pituitary Apoplexy/diagnosis , Pituitary Apoplexy/therapy , Pregnancy , Pregnancy Complications/diagnosis , Pregnancy Complications/etiology , Pregnancy Complications/therapyABSTRACT
Interdigitating dendritic cell sarcoma is a very rare entity in the spectrum of histiocytic and dendritic cell neoplasms that mostly occurs in lymph nodes, generally presenting as solitary lymphadenopathy, but may affect every organ. Among extra nodal sites, cutaneous interdigitating dendritic cell sarcoma is exceedingly rare; to date, only 9 cases have been described in English literature. The mean age at diagnosis was 60 years, with a male-female ratio of 1,5 to 1; clinically, two different modalities of skin presentation have been reported: solitary, represented by a single red-brownish nodular lesion, or diffuse, characterized by multiple nodular lesions in one or more body districts. The extreme rarity of this sarcoma and its morphological similarity to other poorly differentiated tumors may lead to a delay in diagnosis; in particular, cutaneous localization may be difficult to differentiate from follicular dendritic cell sarcoma, Langerhans cell sarcoma, poorly differentiated squamous cell carcinoma and more generally sarcomatoid carcinoma, atypical fibroxanthoma, malignant melanoma and several sarcomas. Immunohistochemistry plays an important role in identifying this rare entity and formulating a correct histological diagnosis, fundamental requirement for choosing the best therapeutic approach. We report herein a further case of an 81-year-old Caucasian woman who presented to the Dermatology Department to remove an asymptomatic skin papule in the left temporal region, clinically diagnosed as dermatofibroma. The overall pathological and immunohistochemical features supported the diagnosis of a malignant dendritic cell tumor, consistent of interdigitating dendritic cell sarcoma.
Subject(s)
Carcinoma , Dendritic Cell Sarcoma, Interdigitating , Sarcoma , Skin Neoplasms , Soft Tissue Neoplasms , Humans , Male , Female , Middle Aged , Aged, 80 and over , Dendritic Cell Sarcoma, Interdigitating/diagnosis , Dendritic Cell Sarcoma, Interdigitating/pathology , Diagnosis, Differential , Skin Neoplasms/diagnosis , Sarcoma/diagnosis , Soft Tissue Neoplasms/diagnosis , Dendritic Cells , Carcinoma/diagnosisABSTRACT
BACKGROUND: Primordial odontogenic tumour (POT) is a novel entity that was described in 2014 and that is included in the group of benign mixed epithelial and mesenchymal odontogenic tumours. In recent years, several papers have added new cases with some clinical and histopathological aspects that slightly differ from those described in the original report. The aim of this systematic review is to update all available data on POT published in the literature and to identify those features of the neoplasm that require further investigation. MATERIALS AND METHODS: A systematic review of literature was conducted using PubMed, Embase, Web of Science and Scopus. Additional sources were also checked. Publications reporting cases with enough clinicopathological information were included, without any time or language restrictions. Histopathological or radiological studies were considered for qualitative analysis. RESULTS: A total of 30 publications were included. Seventeen papers were used for quantitative analysis while 13 papers were used only for qualitative analysis. A total of 18 cases of POT were identified. Some clinical, radiographic, histopathological and therapeutic features were common in all reported cases, while other aspects of the neoplasm were inconsistent through published cases. This inconsistency was particularly remarkable when dealing with the histopathological features of the neoplasm. DISCUSSION: Some issues about POT remain unclear and deserve to be clarified by future reports. The description of the odontogenic epithelium covering the ectomesenchyme is often contradictory, while it remains debatable whether peripheral ameloblastic epithelial islands or hard dental tissue deposition can occasionally occur within the tumour.
Subject(s)
Odontogenic Tumors , Epithelium , Humans , Odontogenic Tumors/diagnosisABSTRACT
Six cases of meningioma showing oncocytic changes are described. The lesions were composed mostly of sheets, nests, and cords of large polygonal cells with finely granular eosinophilic cytoplasm rich in mitochondria. Neoplastic cells showed nuclear pleomorphism with prominent nucleoli. Necrosis and high mitotic rate were present in the majority of cases. Oncocytic differentiation was demonstrated by conventional histology, immunocytochemistry, electron microscopy, and Western-blot analysis. Oncocytic meningiomas showed an aggressive behavior; recurrences were observed in three cases, and invasion of brain cortex was evident in other two cases.
Subject(s)
Adenoma, Oxyphilic/pathology , Meningeal Neoplasms/pathology , Meningioma/pathology , Adenoma, Oxyphilic/chemistry , Adenoma, Oxyphilic/ultrastructure , Aged , Blotting, Western , Female , Humans , Immunohistochemistry , Kidney Neoplasms/pathology , Male , Meningeal Neoplasms/chemistry , Meningeal Neoplasms/ultrastructure , Meningioma/chemistry , Meningioma/ultrastructure , Middle Aged , Retrospective Studies , Salivary Gland Neoplasms/pathologyABSTRACT
A rare case of solid supratentorial haemangioblastoma presenting in a 67-year-old female with psyco-motory lowering, dysphasia and mild haemiparesis is reported and the pertinent literature is reviewed. The distinction between angioblastic meningioma and haemangioblastoma with the non specific radiological findings of this supratentorial uncommon tumour in are also debated.
Subject(s)
Hemangiosarcoma/diagnosis , Supratentorial Neoplasms/diagnosis , Aged , Female , Hemangiosarcoma/diagnostic imaging , Hemangiosarcoma/surgery , Humans , Supratentorial Neoplasms/diagnostic imaging , Supratentorial Neoplasms/surgery , Tomography, X-Ray ComputedABSTRACT
A case of third ventricle cavernous angioma associated with venous angioma is reported. By a transventricular approach, the cavernoma was totally removed with successful preservation of the venous malformation. After review of the literature, the clinical characteristics and the surgical approach to third ventricle cavernous angioma are discussed; the importance of preservation of associated venous angioma is also underlined.
Subject(s)
Central Nervous System Neoplasms/complications , Central Nervous System Venous Angioma/complications , Hemangioma, Cavernous, Central Nervous System/complications , Adult , Central Nervous System Neoplasms/pathology , Central Nervous System Neoplasms/physiopathology , Central Nervous System Neoplasms/surgery , Central Nervous System Venous Angioma/pathology , Central Nervous System Venous Angioma/physiopathology , Hemangioma, Cavernous, Central Nervous System/pathology , Hemangioma, Cavernous, Central Nervous System/physiopathology , Hemangioma, Cavernous, Central Nervous System/surgery , Humans , Magnetic Resonance Imaging , Male , Third Ventricle/blood supply , Third Ventricle/pathology , Third Ventricle/surgeryABSTRACT
A case of a 56-year-old woman that developed subarachnoid haemorrhage from iatrogenic post-traumatic aneurysm of the cortical middle cerebral artery due to a ventricular tap for hydrocephalus is presented. Previous reported cases of postsurgical aneurysms of the cerebral vessels are discussed and the pathogenesis, the clinical course, the outcome and the advisable treatment of this condition are debated.
Subject(s)
Aneurysm, False/etiology , Iatrogenic Disease , Intracranial Aneurysm/etiology , Female , Humans , Middle AgedABSTRACT
The authors describe the case of a 58-year-old man with an history of seizures because of right parietal parasagittal meningioma. Twenty-two months after complete removal of this neoplasm, the patient showed progressive mental deterioration and at CT-scans revealed a right temporal anaplastic astrocytoma which was operated. In literature the association between intracranial meningioma and astrocytoma is reported in 41 cases. After a brief review of the previous cases, the authors debate the clinical presentation, the diagnostic problems, the aetiopathogenetic hypotheses and the best surgical treatment of this association.
Subject(s)
Astrocytoma/surgery , Brain Neoplasms/surgery , Meningeal Neoplasms/surgery , Meningioma/surgery , Astrocytoma/complications , Astrocytoma/pathology , Brain Neoplasms/complications , Brain Neoplasms/pathology , Humans , Male , Meningeal Neoplasms/complications , Meningeal Neoplasms/pathology , Meningioma/complications , Meningioma/pathology , Middle Aged , Tomography, X-Ray ComputedABSTRACT
The Authors describe the case of an intraventricular subependymoma presenting as subarachnoid hemorrhage in a 42-year-old woman. The preoperative and postoperative CT-scans and Magnetic Resonance Images of this rare benign neoplasm are presented. The pathology, the clinical findings and the prognosis of this tumour are discussed.
Subject(s)
Brain Neoplasms/diagnosis , Glioma/diagnosis , Subarachnoid Hemorrhage/diagnosis , Adult , Brain Neoplasms/diagnostic imaging , Brain Neoplasms/pathology , Brain Neoplasms/surgery , Cerebral Ventricles , Diagnosis, Differential , Female , Glioma/diagnostic imaging , Glioma/pathology , Glioma/surgery , Humans , Magnetic Resonance Imaging , Subarachnoid Hemorrhage/diagnostic imaging , Tomography, X-Ray ComputedABSTRACT
The case of a 63-year-old patient with spontaneous cerebrospinal fluid rhinorrhea from a intraethmoidal encephalomeningocele is presented. The patient was asymptomatic until the old age. The preoperative coronal CT-scan and the preoperative and postoperative MRI are shown. The rarity of this onset in an elderly man and the surgical indications of this disease are debated.
Subject(s)
Cerebrospinal Fluid Rhinorrhea/etiology , Encephalocele/complications , Ethmoid Bone/abnormalities , Meningocele/complications , Age Factors , Encephalocele/diagnosis , Encephalocele/epidemiology , Encephalocele/etiology , Encephalocele/pathology , Epilepsy, Generalized/etiology , Ethmoid Bone/diagnostic imaging , Humans , Incidence , Magnetic Resonance Imaging , Male , Meningocele/diagnosis , Middle Aged , Sella Turcica/diagnostic imaging , Tomography, X-Ray ComputedABSTRACT
The Authors report a rare case of isolated sphenoid sinus aspergillosis in a 69-year-old man. The patient had a complete recovery. The preoperative CT-scans and the preoperative and postoperative MRI are shown. The incidence, the pathology, the various clinical presentations, the prognosis and the management of this disease are debated.
Subject(s)
Aspergillosis , Sinusitis/microbiology , Sphenoid Sinus , Aged , Aspergillosis/diagnosis , Aspergillosis/diagnostic imaging , Aspergillosis/epidemiology , Aspergillosis/therapy , Combined Modality Therapy , Fluconazole/therapeutic use , Humans , Incidence , Magnetic Resonance Imaging , Male , Sinusitis/diagnosis , Sinusitis/diagnostic imaging , Sinusitis/epidemiology , Sinusitis/therapy , Sphenoid Sinus/diagnostic imaging , Sphenoid Sinus/surgery , Tomography, X-Ray ComputedABSTRACT
The authors describe the case of a 71-year-old man without signs of phacomatosis with a history of progressive psychomotory lowering and two simultaneous tumors of the olfactory groove and of the cerebellopontine angle, as demonstrated by CT scans. Histologic examinations showed the lesions to be a meningioma and a neurinoma. The rarity and the possible pathogenesis of this association are discussed.
Subject(s)
Cranial Nerve Neoplasms/complications , Meningioma/complications , Neoplasms, Multiple Primary , Neuroma, Acoustic/complications , Olfactory Nerve , Aged , Cranial Nerve Neoplasms/pathology , Cranial Nerve Neoplasms/radiotherapy , Humans , Male , Meningioma/pathology , Meningioma/radiotherapy , Neoplasms, Multiple Primary/pathology , Neoplasms, Multiple Primary/radiotherapy , Neuroma, Acoustic/pathology , Neuroma, Acoustic/radiotherapyABSTRACT
Spinal cord subependymoma is a rare tumour with only 39 reported cases in the literature. The authors report a further case of this neoplasm in a 53 year old man with a progressive paraparesis, paraesthesias of the lower limbs and sphincter disturbance. The tumour was partly removed, without progression 5 years after surgery. After a careful review of the literature, the optimal treatment of this spinal tumour is debated.
Subject(s)
Glioma, Subependymal/pathology , Spinal Cord Neoplasms/pathology , Glioma, Subependymal/physiopathology , Glioma, Subependymal/surgery , Humans , Magnetic Resonance Imaging , Male , Middle Aged , Recovery of Function/physiology , Spinal Cord Neoplasms/physiopathology , Spinal Cord Neoplasms/surgery , Thoracic Vertebrae , Treatment OutcomeABSTRACT
In 1985 the Health Department of the Italian Telephone Company decided to launch an oral health programme for all its employees and their relatives, with the collaboration of the WHO Collaborating Centre of the Clinica Odontoiatrica Ospedale S. Paolo, Milan. The programme started with an epidemiological survey of dental and periodontal condition; following data analysis, the company also contracted with private dentists to provide oral care. Four years later, in 1989, several studies were set up to evaluate the programme. The WHO Collaborating Centre Milan was requested to evaluate the periodontal care given to a sample of persons living in the Milan area. Seventy-seven individuals with established periodontal lesions were selected out of a group of 678 aged between 35 and 44 years examined in 1985. The same periodontal and dental indices used in 1985, CPITN (Community Periodontal Index of Treatment Needs) and DMFT (decayed, missing, filled teeth), were re-evaluated in these 77 persons and information about any periodontal care since 1985 was collected and checked against the reimbursement records of the Telephone Company. There was an increase in the percentage of persons with deep pockets (from 55.8 to 72.7 per cent), and of the mean of sextants affected (from 0.9 to 1.9). These individuals had been treated for dental problems, as demonstrated by an increase in the F component and a reduction of the D component of the DMFT, but had undergone virtually no treatment for periodontal problems. This may be considered as a longitudinal study on the natural progression of periodontal pathology in individuals with established periodontal lesions.
Subject(s)
Periodontal Pocket/epidemiology , Adult , DMF Index , Dental Calculus/epidemiology , Dental Calculus/therapy , Health Services Needs and Demand/statistics & numerical data , Humans , Italy/epidemiology , Periodontal Index , Periodontal Pocket/therapy , Telephone , Urban Population/statistics & numerical dataABSTRACT
Solitary fibrous tumor (SFT) is a rare neoplasm, arising in the adult and more commonly in the pleura. For many years it has been referred to the serous surfaces of the body, namely pleura, peritoneum and pericardium; recently cases arising in mesenchymal organs such as lung, mediastinum, liver and paranasal sinuses were reported. We present a SFT of the nasopharynx, observed in a 41 year-old patient complaining a 6 months history of aural fullness at the right ear. Clinical examination revealed the presence of secretory otitis media and swelling of the lateral wall of the nasopharynx. CT scan and MR showed the presence of a solid mass, with scarce vascularization, extending from the right side of the nasopharynx to the infratemporal and pterigoid fossae. The surgical approach consisted in a facial translocation by the rotation of a maxillary-check flap through different osteotomies; a firm whitish mass not invading the surrounding tissues was identified and enucleated. A definitive diagnosis cannot be made at frozen sections, requiring more accurate processing and immunohistochemical staining. Literature reports fourteen cases of SFT of the upper aero-digestive tracts (nasopharynx, paranasal sinuses, larynx) and some 8 more cases in the head and neck area (thyroid, salivary glands and parapharyngeal spaces). This case report adds a further contribution to support the mesenchymal origin of the SFT.
Subject(s)
Mesothelioma/pathology , Nasopharyngeal Neoplasms/pathology , Adult , Humans , Magnetic Resonance Imaging , Male , Mesothelioma/diagnosis , Nasopharyngeal Neoplasms/diagnosisABSTRACT
The author after a short summary about the morphological classification of head and neck cutaneous carcinomas, stresses the necessity of a strict interface of cooperation between surgeon and pathologist. For a better management of the patient with a cutaneous lesions suspected for malignancy is mandatory to take a biopsy and to indicate in the histological report the exact diagnosis of histotype associated with the morphological features related to prognosis.
Subject(s)
Carcinoma/pathology , Head and Neck Neoplasms/pathology , Skin Neoplasms/pathology , HumansABSTRACT
The numerous studies proving that fluoride administration, mainly via fluoridated water, is undoubtedly the most reliable, efficient and economic technique for the prevention of dental decay are considered. However we should not underestimate the existence of a certain degree of distrust among the public or certain technical and bureaucratic problems which can interfere with the diffusion of this method. The experiments conducted in some countries where water fluoridation has been introduced are also reviewed.