Broj: 9-10
Ispis E-mail

EPIDEMIOLOGIJA OSTEOPOROZE U HRVATSKOJ

EPIDEMIOLOGY OF OSTEOPOROSIS IN CROATIA

 

Descriptors: Osteoporosis – epidemiology; Croatia – epidemiology
Summary. There is no disease registry for osteoporosis and osteoporotic fractures in Croatia. According to the annual report of registered diseases, the number of patients with osteoporosis and osteoporotic fractures increased during the last 10 years. In 2004, 0.70% of all registered diseases in Croatia referred to osteoporosis and osteomalacia. Epidemiological data show that the prevalence of osteoporosis in Croatia is similar to other European countries, while the prevalence and incidence of osteoporotic fractures is somewhat higher. It is estimated that 90 000 men and 77 000 women in Croatia older than 50 years have vertebral fractures. The prevalence is more frequent in older age and in women, although the great number of men (16.2%) were diagnosed as having osteoporosis using ultrasound densitometry. Calcium intake is found to be a dominant risk factor for building-up and maintenance of bone density.

 
Ispis E-mail

p53, bcl-2 i Ki-67 U DIJAGNOSTICI INZULARNOG KARCINOMA ŠTITNJAČE
Prikaz bolesnika s pregledom literature

P53, BCL-2 AND Ki-67 IN THE DIAGNOSIS OF INSULAR THYROID GLAND CANCER
Case report with a review of literature

 

Descriptors: Thyroid neoplasms – diagnosis, pathology; Carcinoma – diagnosis, pathology; Ki-67 antigen – analysis; Proto-oncogene proteins C-bcl-2 – analysis; Tumor suppressor protein p53 – analysis
Summary. The report covers the first case of insular thyroid cancer recorded in Croatian medical literature. A 71-year old female patient presented to our hospital with symptoms of inspiratory stridor. Clinical examination disclosed an expansive tumor mass. US guided FNA indicated anaplastic cancer and total thyroidectomy was accordingly indicated. Patho- histological analysis of H/E biopsies disclosed a tumor mass with a characteristic insular growth pattern of monomorphic tumor cells. Immunohistochemical analysis confirmed diagnosis by a diffuse positive reaction to thyreoglobulin, focally to TTF-1, and scant to cytokeratin, while calcitonin, FVIII, CD34 and LCA were clearly negative. P53 and bcl-2 were expressed in 35.9% and 85% of tumor cells, respectively. The proliferation index for Ki-67 was 4.19. According to our survey we suggest a panel of immunohistochemistry for diagnosing insular cancer. Even if partly present, insular cancer should be mentioned in the pathohistological description because of its prognostic meaning.

 
Ispis E-mail

PRIMARNA PIGMENTNA NODULARNA ADRENOKORTIKALNA BOLEST KAO UZROK CUSHINGOVA SINDROMA U SKLOPU CARNEYEVA KOMPLEKSA

PRIMARY PIGMENTED NODULAR ADRENOCORTICAL DISEASE AS CAUSE OF CUSHING'S SYNDROME ASSOCIATED WITH CARNEY COMPLEX

 

Descriptors: Cushing syndrome – etiology, genetics; Adrenal cortex diseases – complications, genetics; Pigmentation disorders – complications, genetics; Multiple endocrine neoplasia – genetics
Summary. We report a 11 year old girl and two 14 year old boys with Cushing's syndrome due to primary pigmented nodu- lar adrenocortical disease (PPNAD). In these patients, hypercortisolism is a consequence of autonomous cortisol secretion from adrenal glands and is ACTH-independent. Besides PPNAD, the girl had lentigines, spotty pigmentation on her bucal mucosa and lips and she also had schwannoma. One of the reported boys had prolactinoma. Considering this, those two patients fulfill the criteria for Carney complex which is a type of multiple endocrine neoplasia syndromes inherited in an autosomal dominant trait. The other boy had PPNAD but no other obvious signs of Carney complex were noticed. Family study didn't reveal any clinical or laboratory signs of Carney complex in our patients' first relatives. All of our patients under- went bilateral adrenalectomy (in one of the boys laparoscopic surgery was performed). Glucocorticoid and mineralo- corticoid substitution has been started. Adrenal glands were macroscopically normal but pathohistological analysis con- firmed the diagnosis of PPNAD.

 
Ispis E-mail

RADIOLOŠKI PRIKAZ PRIMARNOG LIMFOMA KOSTI – RETROSPEKTIVNA STUDIJA

RADIOLOGIC IMAGING OF PRIMARY BONE LYMPHOMA – A RETROSPECTIVE STUDY

 

Descriptors: Lymphoma – radiography, pathology; Bone neoplasms – radiography, pathology
Summary. The purpose of our study was to retrospectively review imaging appearances of primary bone lymphoma in 13 patients (six males, seven females; mean age 30.6 years) from 1994 to 2006 on plain radiography, computed tomography (CT), magnetic resonance (MR) and scintigraphy. Lytic-sclerotic pattern was noticed in 26 of 36 bone lesions on plain radiography and in 27 of 33 lesions on CT scanning. On MR, lesions were homogeneous and hypointense on T1 weighted images, and inhomogeneous and hypointense, isointense or hyperintense with respect to fat on T2 weighted images. Increased uptake on bone scintigraphy was noticed in six out of eight patients. The most common location of primary bone lymphoma was the pelvis. Pathologic type was non-Hodgkin's lymphoma in 11 patients and Hodgkin’s disease in two patients. Primary bone lymphoma presents as mixed lytic-sclerotic lesions that might cause the soft-tissue mass and bone marrow changes associated with little cortical destruction.

 
Ispis E-mail

SRČANI NATRIURETIČKI PEPTIDI U ZATAJIVANJU SRCA

CARDIAC NATRIURETIC PEPTIDES IN HEART FAILURE

 

Descriptors: Heart failure, congestive – diagnosis, physiopathology; Atrial natriuretic factor – physiology, blood; Natriuretic peptide, brain – blood; Biological markers – blood
Summary. Heart failure is a clinical syndrome characterized by abnormalities of cardiac, skeletal muscle, and renal func- tion, stimulation of the sympathetic nervous system, and a complex pattern of neurohormonal changes. Early diagnosis and treatment of heart failure are important factors in reducing morbidity and mortality associated with the disease. During the past several years many studies have demonstrated that natriuretic peptides are the biochemical markers of choice for diag- nosing and risk stratification of patients with chronic heart failure. The value of natriuretic peptides has already been recog- nized by their inclusion in the recent European guidelines for the diagnosis of chronic heart failure. The natriuretic peptides family is comprised of four peptides, each with common 17 amino acid ring structure. The tissue-specific distribution and regulation of each peptide are different. At present, there is no consensus on the most reliable method for natriuretic peptides assay, although non-competitive immunoassay may be more suitable for clinical routine than competitive assay.

 
Ispis E-mail

LAPAROSKOPSKA KIRURGIJA KOD AKUTNE OZLJEDE TRBUHA

LAPAROSCOPIC SURGERY IN ACUTE ABDOMINAL TRAUMA

 

Descriptors: Abdominal injuries – diagnosis, surgery; Laparoscopy; Spleen – injuries; Liver – injuries
Summary. In the past few years, laparoscopy has been increasingly used in patients with acute abdominal trauma. This metod in experienced hands enables direct eye visualisation of abdominal cavity, ensures accurate and early diagnosis and leads to prompt decision on the therapy. Reviewing the literature, laparoscopy in acute abdominal trauma is a safe and accurate procedure to yield diagnosis, enable laparoscopic interventions and help avoid unnecessary laparotomy. In acute abdominal trauma, laparoscopy is mostly used as a diagnostic method, not so often as a therapeutic method, but an expand- ing range of therapeutic interventions is available. We show our early results with diagnostic and therapeutic laparoscopy from January 1st 2003 to March 31st 2004, stressing therapeutic laparoscopy. We performed 79 laparoscopic explorations in patients with diagnosis of acute abdomen. 7 of them were explored because of acute abdominal trauma. In 3 patients there was no need for intervention after laparoscopic exploration, in 1 patient we electrocoagulates smaller bleeding from the spleen and in other 3 patients we made conversion to open surgery procedure, because of III–IV grade liver or spleen injury. In our group we didn’t have injuries of any other internal abdominal organs. Laparoscopic treatment of acute abdominal trauma with spleen or liver injury is applicable in I–III grade liver injury and I–II grade spleen injury, while in greater injuries it is necessary to make conversion to laparotomy.

 
Ispis E-mail

CERVIKOGENA PROPRIOCEPTIVNA VRTOGLAVICA: ETIOPATOGENEZA, KLINIČKA SLIKA, DIJAGNOSTIKA I TERAPIJA S POSEBNIM NAGLASKOM NA MANUALNU TERAPIJU

CERVICOGENIC PROPRIOCEPTIVE VERTIGO: ETIOPATHOGENESIS, CLINICAL MANIFESTATIONS, DIAGNOSIS AND THERAPY WITH SPECIAL EMPHASIS ON MANUAL THERAPY

 

Descriptors: Vertigo – diagnosis, physiopathology, therapy; Cervical vertebrae – physiopathology; Proprioception
Summary. Cervical proprioceptive system (CPS) consisting of mechanoreceptors of cervical intervertebral joints, mecha- noreceptors of neck muscles and ligament’s insertions, muscle spindles located in deep short muscles of cervical spine and sensitive fibers connecting neck’s proprioceptors with neurons of cornu posteriori of spinal cord, plays an essential part in maintaining bodily balance. CPS, via tractus spinovestibularis, is connected to vestibular nuclei. Clinical and neuro- physiological studies have shown that functional disorders and/or organic lesions of CPS cause identical symptoms as vestibular diseases: vertigo, nystagmus and balance disorders. Dysfunction (functional blockade) of craniocervical joints is the most frequent cause of cervicogenic proprioceptive vertigo (CPV). The constant tension of the capsule of a blocked joint irritates mechanoreceptors protecting the joint’s capsules. The increased activity of mechanoreceptors results in confusion of vestibular system. That is, the impulses from the blocked craniocervical joints do not correspond to the impulses from the vestibular organ and other sensory systems that take part in maintaining bodily balance. The disharmony of impulses results in an inadequate vestibulo-spinal and vestibulo-ocular reaction manifesting as vertigo and nystagmus. Hyperactivity of craniocervical mechanoreceptors also causes disturbances in reflex regulation of postural muscle tonus manifesting as »general instability«. Knowledge of CPV as a separate clinical entity is important from diagnostical and therapeutical aspect. As it concerns a peripheral vestibular disorder still unknown to a wider circle of physicians, the article describes etiopathogenesis, clinical manifestations, diagnosis and therapy of CPV with special emphasis on manual therapy.

 
Ispis E-mail

UPOTREBA MAGNETSKE REZONANCIJE U DIJAGNOZI I PROGNOZI MULTIPLE SKLEROZE

USE OF MAGNETIC RESONANCE IMAGING

 

Descriptors: Multiple sclerosis – diagnosis, pathology; Magnetic resonance imaging – methods
Summary. Multiple sclerosis is an autoimmune disease characterized by demyelination and axonal loss. Conventional magnetic resonance imaging allows the demonstration of spatial and temporal dissemination of multiple sclerosis lesions earlier than is possible from clinical assessments. A variety of conventional magnetic resonance imaging protocols, in conjunction with clinical assessment, are now routinely used to increase the accuracy of diagnosis and long-term prognosis of multiple sclerosis. T2-weighted hyperintense lesions are related primarily to increased water content and thus cannot distinguish between inflammation, edema, demyelination, Wallerian degeneration, and axonal loss, whereas the contrast gadolinium-enhanced lesions on T1-weighted images reflect increased blood-brain barrier permeability associated with active inflammatory activity. Conventional magnetic resonance imaging metrics are not sufficiently sensitive to detect invisible brain damage in the normal appearing brain tissue, and they do not show a reliable correlation with clinical measures of disability. However, numerous studies showed that they can improve accuracy in the diagnosis and prognosis of multiple sclerosis. Recently, non-conventional magnetic resonance imaging techniques have been introduced to increase the accuracy of diagnosis and prognosis of multiple sclerosis. Several studies have used brain atrophy, T1-hypointense lesion volume, magnetization transfer imaging, diffusion-weighted imaging and magnetic resonance spectroscopy to test whether the extent and severity of tissue loss in lesions and in normal appearing gray and white matter at the time of clinically isolated syndrome may have diagnostic and prognostic value. These magnetic resonance imaging techniques represent a powerful tool to non-invasively study different pathological substrates of lesions and microscopic tissue changes. Additional short- and long-term prospective studies are requested to establish their value in the diagnosis and prognosis of multiple sclerosis.

 
Ispis E-mail

NEUROFIBROMATOZA TIP 2 (CENTRALNA NEUROFIBROMATOZA ILI BILATERALNI AKUSTI^KI NEUROMI, VESTIBULARNI [VANOMI): OD FENOTIPA DO GENA

NEUROFIBROMATOSIS TYPE 2 (CENTRAL NEUROFIBROMATOSIS OR BILATERAL ACOUSTIC NEUROMAS, VESTIBULAR SCHWANNOMAS): FROM PHENOTYPE TO GENE

 

Descriptors: Neurofibromatosis 2 – diagnosis, genetics, therapy
Summary. Neurofibromatosis type 2 (NF2) is an autosomal dominant disease that predisposes to bilateral vestibular schwannomas (neurinomas), other central and peripheral nervous system tumours (multiple meningeomas and neuro- fibromas) and ocular abnormalities (cataract). The NF2 tumour suppresor gene is localised on chromosome 22q12 and encodes protein called schwannomin or merlin which is related to a family of cytoskeleton-to-membrane proteins linkers ERM (ezrin-radixin-moesin proteins). About 50% of all cases are new germline mutations, although about 20% of appar- ently sporadic cases represent somatic mosaicism. The majority of observed germline NF2 mutations are point mutations which result in schwannomin with an altered or absent C-terminal domain. NF2 has a variable clinical presentation, with two basic types: severe type having early onset and progressive growth of tumors and the milder type having later onset and less aggressive course. The genotype-phenotype correlations indicate a greater variability of clinical disease expression. In this paper we discuss the epidemiology, genetic and clinical characteristics, diagnostic criteria, investigations, screening for risk persons and recommendations for care and therapy of patients with NF2.

Attachments:
Download this file (NEUROFIBROMATOZA TIP 2 (CENTRALNA NEUROFIBROMATOZA ILI BILATERALNI AKUSTI^KI NEU)NEUROFIBROMATOZA TIP 2 349 Kb
 
Ispis E-mail

ANAFILAKTIČKA REAKCIJA KAO NUSPOJAVA PRIMJENE OPĆIH ANESTETIKA I MIŠIĆNIH RELAKSANSA

ANAPHYLACTIC REACTION AS A SIDE-EFFECT OF ADMINISTRATION OF GENERAL ANESTHETICS AND NEUROMUSCULAR BLOCKING AGENTS

 

Descriptors: Anaphylaxis – chemically induced, diagnosis, therapy; Neuromuscular blocking agents – adverse effects; Anesthesia – adverse effects
Summary. The incidence of anaphylactic reactions during anesthesia is between 1:5000 and 1:25000 anesthetics. During the IgE-mediated anaphylactic reaction mast cells release proteases such as tryptase, histamine and vasoactive mediators. The release of mediators from the mast cells and basophils is responsible for the immediate clinical manifestations of anaphylaxis. Anaphylactoid reactions can be caused directly by a release of histamine and other mediators from mast cells and basophils and they don't depend on interaction of IgE antibodies with antigen. The most frequent agents that cause anaphylactic and anaphylactoid reactions during anesthesia are neuromuscular blocking agents (among them the highest percent refers to rocuronium and succinylcholine), some general anesthetics, antibiotics, blood and blood products, opioids and latex. Increased tryptase concentration in serum is a marker for systemic mast cell activation. Skin tests (in vivo) are used for verification of specific hypersensitivity to drugs in patients after anaphylactic reaction. In vitro tests prove the presence of specific IgE antibodies for drugs. The plan for the treatment of anaphylactic reactions must be established before the event. Airway maintenance, 100% oxygen administration, intravascular volume expansion and epinephrine are essential to treat the hypotension and hypoxia that result from vasodilatation, increased capillary permeability and bronchospasm. As soon as the diagnosis has been made the adrenalin should be given intravenously 1 to 3 ml of 1:10000 aqueous solution (0.1 mg/ml) over 10 minutes. Prevention is possible with methylprednisolone 125 mg i.v. 1 hour before administering of anesthetics and neuromuscular blocking agents with or without antihistaminic chlorpiramine-chloride 1 amp i.v. few minutes before anesthesia.