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Andrzej Marchel

Publications and source records attributed to Andrzej Marchel.

18 recordsLinked to original sources

Gene expression profile as a prognostic factor in high-grade gliomas.

Some clinical factors have been useful in predicting prognosis in high-grade gliomas, however, unexpected differences in survival time have generated attempts to search for more precise parameters. It is clear that tumour behaviour depends mostly on gene alterations. Known single gene alterations failed to accurately define survival time, however, recently, the gene profiling based on microarray technology has raised hopes. Our aim was to assess whether the genetic predictor exceeds clinical parameters in the prognosis of malignant gliomas. We performed gene expression analysis of 28 gliomas (3 grade II, 10 grade III and 15 grade IV, according to WHO classification), and 5 control, normal brain samples, using Clontech oligonucleotide arrays with 3,757 known genes. The signal-to-noise statistics was used to separate classes, and the leave-one-out method was used to assess the smallest number of genes make it clear with a minimal cross-validation error. All gliomas, or only high-grade tumours, were clearly separated from the normal brain samples using 7 or 9 most differentially expressed genes. Hierarchical clustering failed, but the fuzzy c-means method was useful in high-grade gliomas to find a gene prediction model, which, with clinical factors, was assessed in survival analysis. Univariate analysis demonstrated that age, WHO grade (IV vs. III), radiation dose (> or = 50 Gy vs. 42 Gy), postoperative KPS score (100 points vs. others), neurological deficit as the first sign of the disease vs. others, and gene expression profile were significant predictors of survival. In multivariate analysis, the gene expression profile remained the only independent predictor (p = 0.007). Thus, our conclusion is that gene expression pattern predicts outcome in high-grade gliomas independently of other factors.

Adult↗

Recommendations for the management of intracranial haemorrhage - part I: spontaneous intracerebral haemorrhage. The European Stroke Initiative Writing Committee and the Writing Committee for the EUSI Executive Committee.

This article represents the recommendations for the management of spontaneous intracerebral haemorrhage of the European Stroke Initiative (EUSI). These recommendations are endorsed by the 3 European societies which are represented in the EUSI: the European Stroke Council, the European Neurological Society and the European Federation of Neurological Societies.

Emergency Medical Services↗

Chordoid meningiomas of a different histopathological pattern: a report of two cases.

Chordoid meningioma is an uncommon histopathological variant of meningioma with a peculiar chordoma-like appearance. Its association with systemic inflammatory disorder linked to Castleman's syndrome was confirmed in the majority of young patients, however such a relationship in adults remains enigmatic. We report two cases of chordoid meningiomas in adult patients without manifestation of Castleman's syndrome. One tumour was almost totally composed of chordoma-like areas whereas the second one exhibited the unique combination of chordoma- and chondroma-like pattern. This is the first description of chordoid meningioma combined with extensive cartilaginous metaplasia. Both tumours exhibited histological evidence of infiltrative growth, accompanied by a relatively high proliferative index within structures of chordoid appearance. The designation of the chordoid component in meningioma is very important as this subtype of meningioma exhibits a more aggressive biological behaviour and higher risk of recurrence.

Cartilage↗

[Sudden deafness as a presentation of acoustic neuroma].

Sudden deafness (SD) is thought to be a heterogenic group of disorders as to etiopathogenesis. Acoustic neuroma should always be considered in the differential diagnosis. The authors analysed symptoms occurring in the group of 89 patients, diagnosed with acoustic neuroma. A special attention was paid to the role of sudden deafness as a clinical manifestation of the VIIIth nerve pathology. Progressive hearing loss, tinnitus, headache and sudden deafness were the most common complaints. Sudden deafness was developed by approximately 1 of the investigated patients (24.7%). Progressive hearing loss, tinnitus and sudden deafness were also dominating initial signs. The sudden deafness onset was preceded by the period of progressive hearing loss in 3 patients. In one case episode of SD occurred twice.

Adolescent↗

[The visual acuity impairment as the only sign of cerebral aneurysms--case report].

Cerebral aneurysms are the most common reason of subarachnoid haemorrhage at the age of 50-60. Though the results of such haemorrhage are severe (high morbidity and mortality), it is quite often, the first noticeable sign of the problem. Previous symptoms i. e. headache, ophthalmic disturbances, temporary neurological symptoms are often passed over. The authors present the case of a young woman with cerebral aneurysms, in which the visual acuity impairment was the only symptom of the disease.

Adult↗

Very late relapse of medulloblastoma.

A case of 47-year-old woman with a local relapse of medulloblastoma 23 years after initial presentation is reported. At the age of 24, the patient underwent resection of medulloblastoma of the right cerebellar lobe, followed by the craniospinal orthovoltage irradiation (3600 R to the brain, and 3000 R to the spinal cord). At the 21st year of follow-up, a second cancer originating in the thyroid gland was diagnosed. Thyroidectomy followed by 131-iodotherapy for the papillary cancer was performed. Two years later she was operated for the recurrence of medulloblastoma at the former site. The patient was unfit for chemotherapy due to poor bone marrow reserve following the previous treatment. The reirradiation of the posterior cranial fossa was performed postoperatively. The patient was given 45 Gy in 25 fractions to the recurred tumour volume with 2 cm margin within 41 days. The treatment was performed by 6 MV photons with conformal technique and noncoplanar beams arrangement. The patient is disease free 15 months after relapse of medulloblastoma. The following problems are discussed: late relapse of medulloblastoma, secondary cancers after craniospinal irradiation, and retreatment of CNS tumours.

Adult↗

[Treatment of petrosal cholesteatoma with intracranial extention].

The authors describe various methods of surgical treatment of extensive petrous pyramid cholesteatoma. The surgical technics were selected to each individual patient. The approach depended on the disease's course, the lesion extention and the ear functional state. Total removing of cholesteatoma were possible by the lateral petrosectomy or by the middle fossa approach. The authors underline that petrous cholesteatoma can develop after previous radical mastoidectomy. The origin of this type of cholesteatoma is usually supratubal recess.

Aged↗

[10 years survival of patient with lung cancer and cerebral metastasis].

The authors describe the case of survival for the period of 10 years after brain metastasis surgery and removal of the left lung upper lobe due to adeno-squamous cells carcinoma. Surgery did not generate any complications. Within 8 years after the surgery the radiological examination showed infiltrations resembling changes typical for tuberculosis. Microbiological analysis showed a culture of Mycobacterium kansasi leading to diagnosis of mycobacteriosis. Hence the antituberculous treatment was extended to 12 months to be interrupted due to liver damage. Two years later the patient experienced incident of haemoptysis. Detailed examination and assessment of the respiratory tract condition revealed COPD without features of renewal of the neoplastic process or infection by Mycobacterium tuberculosis or mycobacterium other than tuberculosis. This case demonstrates that aggressive surgical approaches to lung cancer with solitary cerebral metastasis significantly improve patient survival and justifies its widespread use.

Adenocarcinoma↗

Expression of macrophage/histiocytic antigens in pleomorphic xanthoastrocytomas.

Pleomorphic xanthoastrocytoma (PXA) is a rare variant of a superficial cerebral astrocytoma characterised by distinct clinical and histological features. Its derivation from subpial astrocytes has been proposed, although the capacity of neoplastic cells for expression of different immunohistochemical markers is still under debate. These immunohistochemical studies were performed on eight cases of PXA in order to evaluate the expression and co-expression of glial and macrophage/histiocytic markers in various tumour cell populations. The expression of antigens was examined with the use of single- and double-immunolabelling methods for GFAP, vimentin, LCA, CD68, HLA-class II and MAC 387. All the cases of PXA showed variable immunoreactivity to GFAP, both in spindle-shaped and pleomorphic lipidised tumour cells. A subset of neoplastic cells was stained strongly with HLA-class II monoclonal antibody and with antibody to CD68. The reactivity to LCA and MAC 387 was absent in neoplastic cells, while it was easily evidenced in the non-neoplastic infiltrative component. The immunohistochemical double staining demonstrated the co-expression of GFAP and HLA-class II or CD68 antigens in the cytoplasm of individual neoplastic cells, including large pleomorphic, lipid-laden ones. It seems that tumour cells in PXAs derived from subpial astrocytes reveal monocyte/macrophage immunophenotype and demonstrate the capability of functional behaviour as mesenchymal cells with phagocytic activities. The variability in expression of antigens related to glial and monocytic/macrophage differentiation stressed the immunophenotypic heterogeneity of tumour cells in PXAs.

Adolescent↗

[Results of treatment of non-traumatic cerebellar haemorrhages].

AIM: Presentation of experiences in the treatment and tentative determination of factors of prognostic importance which could be useful in the selection of appropriate treatment of patients with non-traumatic cerebellar haemorrhage. MATERIAL AND METHOD: 35 consecutive patients treated in the years 1987-1996 were analysed retrospectively. Their condition on admission was assessed using Glasgow Coma Scale and the treatment results were assessed using the Glasgow Outcome Scale at the time of discharge. All patients had CT which was repeated, as necessary, and in some cases angiography was done. Ten patients were treated surgically and 25 only conservatively (in six of them temporary external ventricular drainage was performed due to hydrocephalus). The analysis included the influence of localisation and volume of haemorrhage, presence of hydrocephalus, intraventricular extension of haemorrhage fourth ventricle and quadrigeminal cistern appearance on the state of the patients and on treatment results. Non-parametric tests: Mann-Whitney and variance analysis of Kruskal-Wallis were used for determination of statistical significance (p < 0.05). RESULTS: Six patients were in coma (4-7 GCS score), 6 had GCS score 8-12, 6 had GCS score 13-14, and 17 patients had no consciousness disturbances. Haematoma involved only cerebellar hemisphere in 21 cases, hemisphere and vermis in 12, cerebellum with brain stem extension in 2 cases. Haematoma volume was below 20 ml in 25 cases, over 20 ml in 5 cases, and in 5 case the volume could not have been determined. Hydrocephalus was present in 12 patients being related to CSF outflow block in 7 and to intraventricular haemorrhage in 5 cases. Intraventricular extension of haemorrhage occurred in 9 cases. Hydrocephalus presence (p = 0.005) and haematoma volume (p < 0.03) influenced significantly consciousness level on admission. In the surgically treated group 2 patients died and in 7 cases the result was satisfactory (GOS:MD + GR). In the group treated conservatively 4 patients died, 2 became disabled, and 19 left the hospital in good or very good condition (GOS:MD + GR). The total mortality was 17.2%, consciousness level on admission (p = 0.001), haematoma volume (p < 0.05), hydrocephalus presence (p < 0.008), intraventricular extension of haemorrhage (p < 0.008) had significant influence on treatment results. CONCLUSIONS: In the light of our experience it is suggested that patients in coma should be operated on for haematoma evacuation with or without temporary external ventricular drainage. In conscious patients with stable course of disease medical treatment can be considered.

Adult↗

[Results of treatment of cerebellar infarctions].

PURPOSE: The aim of this study is to assess the treatment results in patients with cerebellar infarctions and attempt to determine the features influencing the results. MATERIAL AND METHODS: We have analysed 12 patients with cerebellar infarctions treated from 1987 to 1996. The patients were admitted to hospital in the period between 24 hours and 37 days after onset. The level of consciousness on admission was assessed according to the Glasgow Coma Scale and results of treatment were assessed according to the Glasgow Outcome Scale at the time of discharge. The CT, MR, angio-MR, cerebral arteriography, USG-Doppler and ECHO were the main diagnostic methods. All patients were treated medically; temporary external ventricular drainage or ventriculoperitoneal shunt were used when hydrocephalus had been found. The influence of the level of consciousness, stroke localisation and presence of hydrocephalus on the results of treatment were analysed. RESULTS: 2 patients were in coma on admission, 3 patients scored 13-14 points in GCS and 7 patients did not demonstrate any consciousness disturbances. On neurological examination patients showed cerebellar signs in 9 cases, hemiparesis in 4 cases, lower cranial nerve dysfunction in 3 cases, eyeball movement disorders, compulsory gaze deviation, hemihypoaesthesia, trigeminal nerve dysfunction, peripheral facial palsy in 2 cases each and deafness in 1 case. Infarctions were localised in the cerebellar hemisphere only in 7 cases, in the cerebellar hemisphere with vermian extension in 2 cases and in 3 cases in cerebellum with brain stem extension. Based on additional investigations atherosclerotic occlusion in 3 cases and embolism mechanism in 4 cases were found as causes of the stroke; in 5 cases the cause of stroke remained unknown. The hydrocephalus resulting from the obstruction of cerebrospinal flow pathways was found in 5 patients. 1 patient died, permanent neurological deficits (GOS: SD) were found in 2 patients, the treatment results were successful (GOS: MD + GR) in 9 patients. The infarctions with brain stem extension had the greatest influence on treatment results among all analysed features. The level of consciousness on admission and presence of hydrocephalus had less influence on treatment results. CONCLUSIONS: In all patients with consciousness disturbances the hydrocephalus was found. The stroke localisation had a great influence on treatment results: worst results were obtained in patients with infarcts extending onto the brain stem. The consciousness disturbances on admission and the presence of hydrocephalus had only a slight influence on the results of treatment.

Antihypertensive Agents↗

[Arachnoid cysts of the middle cranial fossa presented as subdural hematomas].

The aim of the study was to present the authors' own experience and discuss the treatment method of arachnoid cysts of the middle cranial fossa disclosed as subdural hematoma. Three cases of male patients operated on because of chronic subdural hematoma are presented. Control CT studies after evacuation of hematomas revealed arachnoid cysts of the middle cranial fossa and all patients were qualified for delayed cystocisternostomy by open craniotomy. Indirect signs of presence of arachnoid cysts in the form of bony abnormalities and expanded the middle cranial fossa in the first CT were seen in all patients. Cysts were asymptomatic until the injury in all cases. The volumes of cysts in MRI scans were: 17.8 ml, 52.9 ml and 92.4 ml, respectively. All cysts were type II according to Galassi classification. After control MRI described above made to evaluate cyst appearance, delayed cystocisternostomy to basal cisterns was undertaken in two cases with full success. No complications were observed. The third patient refused surgery. During surgery the thick and non-transparent medial cyst wall and arachnoidea of tentorial notch cisterns were observed impeding the exact identification of neurovascular structures. In our opinion arachnoid cysts of the middle cranial fossa revealed as subdural hematoma should be operated on in two stages: in the first step subdural hematoma should be evacuated and in the second step cystocisternostomy should be performed. With regard to observed morphological changes of arachnoidea and cyst walls we think that open cystocisternostomy is treatment of choice in these cases.

Adult↗

[Clinical symptoms of the supratentorial arteriovenous malformations and factors influencing their occurrence].

BACKGROUND AND PURPOSE: The aim of this study was to assess frequency of main symptoms of the supratentorial arteriovenous malformations (AVM) and attempt to find factors influencing their occurrence. MATERIAL AND METHODS: 88 consecutive patients operated on for AVM located supratentorially in the years 1983-2000 were included in a retrospective analysis. Statistical analyses including chi-square test and exact Fisher test were performed for comparisons among groups. RESULTS: The most common cause of diagnostics was intracranial hemorrhage--62.5%. Epilepsy, headaches and non-hemorrhagic focal deficits were described in 38.6%, 9.1% and 4.5%, respectively. Deterioration (focal deficits and/or disturbances of consciousness) after hemorrhage occurred in 30%. The risk of hemorrhage from AVM was 2.2% per year. Hemorrhage was more frequent in the cases of small size (<3 cm) of AVM (p=0.001), deep location (p<0.05) and when single (p=0.001) and exclusively deep (p<0.05) venous drainage were present. However, superficial location of AVM and nidus size >3 cm significantly influenced epilepsy occurrence (p<0.05 and p=0.001, respectively). Sex and coexisting aneurysm did not influence occurrence of epilepsy or hemorrhage. CONCLUSIONS: Supratentorial AVMs manifest most common as intracranial hemorrhage and epilepsy. Factors increasing the risk of hemorrhage are: small size, deep location of AVM, single and exclusively deep venous drainage. Factors increasing the risk of epilepsy are: superficial location and size >3 cm.

Adolescent↗

[The microsurgical treatment of the supratentorial arteriovenous malformations. Part I--early and late results].

BACKGROUND AND PURPOSE: The aim of this study was an analysis of early and late results of the microsurgical treatment of arteriovenous malformations (AVM) located supratentorially and factors that may influence the outcome. MATERIAL AND METHODS: 88 consecutive patients operated on in the years 1983-2000 for supratentorial AVM located were included in a retrospective analysis. All patients underwent microsurgical selective removal of AVM without prior embolization. The outcome was assessed on the day of discharge according to the Glasgow Outcome Scale (GOS) and at least 6 months after surgery according to the Karnofsky Scale (KS). RESULTS: A satisfactory outcome (GR+MD in GOS) was achieved in 92%. A severe deficit appeared in 4.5% and 3 (3.4%) patients died. The only factor influencing satisfactory outcome was low grade of AVM (I-II) in the Spetzler-Martin scale (p<0.0001). Factors influencing the excellent outcome (GR in GOS) are: size of AVM<3 cm (p=0.02), non-eloquent location (p=0.001) and exclusively superficial venous drainage (p=0.04). There was no case of deterioration in the late period. In 3/4 of patients discharged with deficit, a significant improvement was observed: a mild deficit withdrew in 13 of 17, and a severe deficit withdrew in 3 of 4. A satisfactory outcome in final assessment (KS>70%) was achieved in 95.5%, severe disabling deficit (KS 50%) remained in 1.1%. CONCLUSIONS: Results of the surgical treatment of AVM are satisfactory, especially in I and II grade of the Spetzler-Martin scale. In these cases microsurgical removal should be the method of choice, because immediately after treatment the risk of further hemorrhage is eliminated. Postoperative deficits withdraw during weeks or months in most cases and the final satisfactory result was achieved in 95% of patients.

Adolescent↗

[The microsurgical treatment of the supratentorial arteriovenous malformations. Part II--complications].

BACKGROUND AND PURPOSE: The aim of this study was an analysis of complications after surgical treatment of the cerebral supratentorial arteriovenous malformations (AVM), assessment of their clinical sequelae, and attempt to find factors influencing their occurrence. MATERIAL AND METHODS: 88 consecutive patients operated on for AVM in the years 1983-2000 were included in a retrospective study. In all patients microsurgical, selective removal of AVM was performed, without prior embolization. The statistical analysis was carried out by means of exact Fisher test and c2 test. RESULTS: Complications in the postoperative period were observed in 45.5%, including short-term deterioration (27.3%) and symptoms present till the day of discharge (18.2%). Mechanisms of deterioration were as follows: significant intraoperative hemorrhage (5.7%), hemodynamic disturbances after AVM removal (20.5%) and resection of AVM in the eloquent area (19.3%). Many variables that may contribute to the complications were studied. Factors increasing the risk of significant intraoperative hemorrhage are: steal effect visible in angiography (32% vs. 10%, p<0.05), intraventricular penetration of AVM (38% vs. 11%, p<0.05). Factors increasing the risk of hemodynamic disturbances are: feeding from the medial cerebral artery (MCA) (31% vs. 8%, p=0.02) and complex venous drainage (32% vs. 14%, p=0.05). CONCLUSIONS: The most common causes of postoperative deterioration are hemodynamic disturbances after AVM removal and manipulation in the eloquent area. Hemodynamic disturbances worsened the prognosis significantly, and were the only cause of mortality (3.4%). However, massive intraoperative hemorrhage and operation in the eloquent area did not influence the outcome significantly. Risk factors for intraoperative hemorrhage are steal effect and intraventricular penetration of AVM. Risk factors for hemodynamic disturbances are feeding AVM from MCA and complex venous drainage.

Adolescent↗

[Long-term result of the surgical treatment of craniopharyngiomas].

BACKGROUND AND PURPOSE: The aim of the study was to assess the long-term outcome in patients with cranipharyngioma, depending on the extent of tumour removal. MATERIAL AND METHODS: Thirty-six patients (17 females and 19 males), aged between 10 and 57, were treated at the Clinic of Neurosurgery of the Medical University of Warsaw between 1990 and 2004. The most common initial symptoms included: decreased visual acuity in 75% of cases, visual field defect in 69% of cases, headaches in 58% cases and endocrine disorders in 50% of cases. The initial diagnosis was based on two-phase computed tomography (CT) and magnetic resonance imaging (MRI). The most common means of surgical access was by pterional craniotomy, which was used in 27 cases. Due to tumour localisation, other accesses (bifrontal - basal, transventricular and transsphenoidal) were also used. RESULTS: The tumour removal was considered total in 31%, subtotal in 38%, and partial in 31%. In the post-operational period 2 patients died. Control examinations were performed to investigate long-term outcome: two-phase MRI or CT, evaluations of visual acuity and visual field. During the follow-up period, tumour recurrence occurred in 1 patient (9%) following complete tumour removal, in 8 patients (57%) after subtotal removal, and in 6 patients (55%) after partial removal. The range of follow-up was between 2 and 14 years. CONCLUSIONS: On the basis of our own experience we conclude that complete removal of the craniopharyngioma leads to the best outcome in terms of survival time and period free of recurrence. Clinical and radiological observation of the patients who underwent nonradical operation seems to be reasonable. In cases with tumour recurrence, reoperation and subsequent radiotherapy are advisable.

Adolescent↗

[Operative treatment of anterior cranial base meningiomas].

BACKGROUND AND PURPOSE: The aim of the study is to assess outcome of surgical treatment of anterior cranial base meningiomas with special emphasis on the evaluation of visual skills after surgery. MATERIALS AND METHODS: A series of 52 consecutive patients operated on for anterior cranial base meningioma in the last ten years is reported. 18 patients had decreased visual acuity on admission, 6 experienced blindness in one eye, and 4 were totally blind; defects of visual fields were found in 17 patients. Primary optic atrophy and secondary optic atrophy were noted in fundcoscopy in 20 and 2 patients, respectively. Papilloedema was found in 3 patients. RESULTS: Meningiomas were resected radically (Simpson I surgery) in 13 patients and in 34 patients Simpson II surgery with coagulation of the dural attachment was made; meningiomas were partially removed in 5 patients (Simpson IV surgery). In one patient dense hemiparesis occurred after the surgery, and 3 others presented adynamic syndrome, one of whom made a good recovery in follow-up examination. Two patients died: the first one due to a large brain oedema and the second one due to myocardial infarction after uncomplicated postoperative course. The postoperative course in the other 46 patients was uneventful with good outcome. Visual acuity improved in 15 cases and did not change in 10 patients; visual acuity further decreased in 3 patients. CONCLUSIONS: Visual recovery is significantly related to preoperative visual acuity values of no less than 0.3 D and to the presence of normal optic discs on fundoscopic examination additionally tumour size less than 3.5 cm favourably affects visual prognosis in meningiomas of tuberculum sellae.

Adult↗