Chondroblastic osteosarcoma of the nasal cavity: an exceptional and misdiagnosed presentation.

Chondroblastic osteosarcoma of the nasal cavity is a rare and aggressive tumor that presents diagnostic challenges due to its variable clinical and radiological features. Histological analysis is crucial for an accurate diagnosis, despite morphological similarities with chondrosarcoma. We present a case of primary craniofacial chondroblastic osteosarcoma originating from the nasal cavity in a 17-year-old adolescent. The tumor was characterized by cartilaginous lobules and spindle cell proliferation with osteoid matrix deposition. Immunohistochemical analysis supported the diagnosis. This case highlights the rarity of this particular presentation and emphasizes the significance of accurate diagnosis through histopathological evaluation to achieve optimal management.

["Factitious disorder and skin picking: Clinical approach". A case report]. / Trouble factice et dermatillomanie : approche clinique. À propos d'un cas.

OBJECTIVE: The number of patients requiring primary and secondary care for factitious disorder unexplained by any known medical condition is high. We report a case illustrating the clinical and psychopathological features of factitious disorder. The treatment difficulties encountered in the association of this disorder with dermatillomania are discussed. CASE REPORT: The patient was a 22-year old girl with abrasions on the face and forearms with ingested epidermal layer of the skin. She also had multiple somatic complaints, the authenticity of which was difficult to confirm. The diagnosis of comorbid factitious disorder with dermatillomania was retained. In view of reducing self-harm acts, we prescribed a mood stabilizer associated with an anxiolytic for 6 months. The self-harming acts have regressed, while the hypochondriacal complaints remain with a tendency of overstatement. DISCUSSION: Factitious disorder (FD) is a mental disorder occurring in patients acting intentionally similar to a physically or mentally sick person with no apparent benefits. The reported cases often show FD comorbidity with other psychiatric disorders such as substance abuse, somatoform disorders, dysthymia, borderline personality disorder and sexual disorders. Comorbidity of factitious disorder with neurotic excoriation is exceptional, and rarely described in the literature. Pathological skin picking (PSP) is a disabling disorder characterized by repetitive skin picking, which causes tissue damage. It was estimated to affect 2% of the population. PSP is currently listed as an impulse control disorder not otherwise specified, it is associated with a high rate of psychiatric comorbidity like borderline personality disorder. CONCLUSION: The comorbidity of factitious disorder and dermatillomania makes diagnosis very difficult. The limit between the two disorders is sometimes unclear.

[Aneurysmal cyst of ethmoid bone: a case report]. / Le kyste osseux anévrismal de l'ethmoïde : à propos d'un cas.

AIM: To report on the value of imaging in the diagnosis and assessment of aneurysmal cyst of the ethmoid bone. CASE: A 12-year-old girl with a stuffy nose, revealing an aneurysmal bone cyst of the ethmoid, explored by CT, MRI, who had a preoperative arteriography with embolization. CONCLUSION: Aneurysmal bone cyst is a benign bone lesion which rarely involves the facial bones. Imaging plays an important role in the diagnostic approach, the assessment of the lesions, and the treatment using the techniques of interventional radiology.

A rare localization of meningioma: meningioma of the foramen of Monro.

Intraventricular meningiomas (IVM) are rare tumors, constituting only 0.5 to 2% of all intracranial meningiomas, and meningiomas localized within the foramen of Monro are exceptional, with only a very few cases reported in the literature. We report the case of a 41-year-old man, admitted to our department for headaches. MRI found a mass tissular well enhanced after gadolinium injection, arising in the region of the foramens of Monro, and extended to the lateral and the third ventricles. Histological examination revealed a meningioma.

[Primary hydatid cyst of the parotid gland]. / Kyste hydatique parotidien primitif.

INTRODUCTION: The hydatid cyst is an anthropozoonosis due to the development of the Echinococcus granulosus tapeworm larva in humans. Its intraparotid localization is extremely rare. CLINICAL CASE: A 10-year-old-male patient was admitted for an isolated renitent swelling of the left parotid region having grown for several months. Cervical ultrasonography revealed a left parotid cystic mass, characterized by a double wall, and a small daughter cyst. The CT-scan typically showed the absence of enhancement after iodine contrast medium injection. The imaging-based diagnosis of a hydatid cyst was supported by positive hydatid serology, and confirmed by histological analysis of the cyst. No other hydatid location was found (chest and abdominal). DISCUSSION: In spite of its rarity, hydatid cyst can be a diagnosis in case of parotid cystic masses. Ultrasonography is the first examination to be performed; it must be completed by CT-scan or even better by MRI. Once the diagnosis of hydatid cyst is confirmed, a chest radiograph and an abdominal ultrasonography should be performed, to screen for other localizations. Surgical resection is the gold standard treatment.

Primary laryngeal tuberculosis mimicking laryngeal carcinoma: CT scan features.

Laryngeal tuberculosis is a rare disease. It is almost always associated with pulmonary tuberculosis. It occurs generally in adults without BCG vaccination or in cases of the acquired immune deficiency syndrome. On laryngoscopy and imaging, it often simulates laryngeal carcinoma, and confirmation is always histological. We report the case of a 36-year-old man who presented to our hospital with dysphonia and dysphagia. Laryngoscopy revealed a lesion of the left vocal cord and the ventricular strip. CT scan found focal, regular thickening of the left vocal cord, associated with irregular thickening of the posterior laryngeal wall. A biopsy confirmed the diagnosis of tuberculosis.

[Os odontoideum: clinical and radiological aspects]. / Os odontoïdeum : aspects cliniques et radiologiques.

Few reports of os odontoideum have been made. We report two cases where this affection was revealed by cervical pain and hemiparesis in one case and acute tetraparesis in the other. Patients with os odontoideum usually present with neurological signs, but some have only cervical pain and some others remain asymptomatic. Radiological exams, including radiograms, cervical scanner and MRI lead to the diagnosis. Different surgical treatment can be proposed to symptomatic patients. Prophylactic surgical treatment is not indicated.

[Hemoptysis revealing a pulmonary arterial aneurysm on Behçet disease in children: role of computed tomography]. / Hémoptysie révélant un anévrysme artériel pulmonaire sur maladie de Behçet chez un enfant: rôle de la tomodensitométrie.

Behçet's disease is a systemic condition whose discovery during hemoptysis on a pulmonary artery aneurysm is rare, especially in children. Through the case of a 11-year-old boy, the authors emphasize the importance of imaging in diagnosis of this disease, whose progression can be fatal if hemoptysis is violent.

[Thumb acrometastasis revealing lung adenocarcinoma: a case report with review of literature]. / Acrométastase du pouce révélant un adénocarcinome pulmonaire: a propos d'un cas avec revue de la littérature.

Bone metastases in the hand and foot bone (acrometastases) are rarely observed. The authors report a case of a 57-years-old man diagnosed as hand tumour, revealing a bronchic adenocarcinoma. Radiography showed destruction of the phalanx, and histology study confirmed a metastasis of the lung cancer.

[Neuro-imaging of tuberous sclerosis]. / Neuro-imagerie de la sclérose tubéreuse de Bourneville.

Tuberous sclerosis is a phakomatosis with central nervous system manifestations characterized by 4 lesions detectable on neuro-imaging: tubers, white matter abnormalities, subependymal nodules and subependymal astrocytomas. The first three are benign lesions composed of by identical cytological lesions varying only in size and location. At CT, enhancement of subependymal nodules is usually considered as evidence of transformation to subependymal giant cell astrocytoma. This latter poses the problem of its relative benignity: hydrocephalus source of morbidity or even mortality. From a series of 22 cases, the authors review the characteristics of these abnormalities.

[Isolated congenital left ventricular diverticulum: report of a paediatric case]. / Le diverticule cardiaque gauche congénital isolé: à propos d'un cas pédiatrique.

Congenital cardiac diverticulum is a rare malformation formed by an outpouching of the ventricular wall, in particular the left ventricle. The thoraco-abdominal type is more frequent than the isolated thoracic type. Topographical and imaging considerations regarding an isolated congenital left ventricular diverticulum incidentally discovered in a 9-year-old-boy are reviewed.