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Biomedical subjects

P Martanovic

Publications and source records attributed to P Martanovic.

11 recordsLinked to original sources

[Thymic cyst--an uncommon cause of neck swelling in children].

The thymus cyst, which is difficult to recognize before the operation may occur in children as a painless swelling of the neck An asymptomatic course of about 100 cases has been reported in the English-written literature until 2002. The cyst is localized along the thymopharyngeal duct, i.e. from the mandible angle to the upper mediastinum. The authors describe cases of two patients. In the male patient the swelling resembled pathologically enlarged lymphatic nodes implicating malignant lymphoma. In the female patient the palpation examination of the swelling suggested the presence of lymphangioma. The radiological examination revealed a cystic formation or a liquefied lymphatic node. The operation on the patients revealed polycystic formation containing a clear brown liquid. Histological examination proved the formation to be a thymus cyst. The neck swelling in children may also be caused by developmental errors--a lateral cyst from the brachial arc, lymphangioma, hemangioma, medial cyst, thyroid gland cyst, parathyroid gland cyst, aberrant or ectoscopic thyroid gland, struma, laryngocoele, lymphatic nodopathy, pathologically changes salivary glands, phlegmona or abscess in the parapharyngeal space, teratoma on the neck, benign tumors (dermoid, epidermoid, neurofibroma, lipoma, lymphoma) and malignant tumors (sarcoma, lymph node metastases). The available literature does not describe any case of thymus cyst of the neck, which should be considered in differential diagnosis of swelling of the neck in children diagnosed before the operation. The final diagnosis may be established only after histological examination. Surgical extirpation is the primary therapy of the neck thymus cyst. The authors describe embryology, histology, present a survey of literature and deal with differential diagnosis, diagnosis and therapy of the neck thymus cyst in children.

Child↗

Morphological variations of secundum-type atrial septal defects: feasibility for percutaneous closure using Amplatzer septal occluders.

The aim of the study was to assess the morphology of secundum-type atrial septal defects (ASD) with a view to percutaneous closure using Amplatzer septal occluders (ASO). One hundred and ninety patients who underwent closure of isolated secundum-type ASD between September 1995 and January 2000 were included. The morphology of the defects was studied using transthoracic and transesophageal echocardiography. Patients with defects of suitable morphology and size underwent percutaneous closure using ASO. The remaining patients underwent surgical closure. Centrally placed defects were observed in 46 patients (24.2%). Morphological variations of secundum-type ASD were detected in 144 patients (75.8%). One hundred and fifty-one patients (79.5%) underwent percutaneous closure using ASO. Thirty-nine patients (20.5%) underwent surgical closure. Centrally placed defects, defects with deficient superior anterior rim, multiple defects, and perforated aneurysms of the interatrial septum are morphological variations of secundum-type ASD suitable for percutaneous closure using ASO. Cathet Cardiovasc Intervent 2001;53:386-391.

Adolescent↗

[A method of paraffin impregnation and its use in morphologic studies of organs].

The authors present a method of paraffin infiltration applied to heart specimens. They describe the dissection, trimming and fixation of the specimen which is followed by common tissue dehydration and infiltration by paraffin wax. Thus preserved permanent specimen allows both retaining the entire organ and visualizing its particular structures.

Heart↗

Developmental defects and chromosomal aberrations in spontaneous abortions and stillbirths.

The authors analysed 1488 cases of spontaneous abortions and stillbirths in Bratislava. They focused on the course of human embryogenesis and the chromosomal constitution. A high mean frequency rate of both developmental defects (14.4%) and chromosomal aberrations (33.6%) was revealed and both were found to be in close relation with the length of gestation. The most severe developmental defects occurred mostly in early stages of human embryogenesis, i.e. in the 1st trimester of gestation.

Abortion, Spontaneous↗

Pathologic anatomy of corrected transposition of the great arteries: medical and surgical implications.

BACKGROUND: Because the double-switch operation (atrial switch plus arterial switch) has recently become feasible in selected patients with congenitally physiologically corrected transposition of the great arteries, a detailed understanding of the pathologic anatomy is now mandatory for cardiologists, radiologists, and surgeons. METHODS: A detailed study of the pathologic anatomy, the clinical implications, and the surgical implications was undertaken on 33 postmortem cases with two ventricles. A companion study was also performed of 44 postmortem cases with functionally only one ventricle. Hence this was an investigation of 77 postmortem cases. RESULTS: Three main anatomic types of corrected transposition of the great arteries (TGA) with two ventricles were found: (1) TGA with solitus atria (S), L-loop ventricles (L), and L-TGA (L), that is, TGA [S,L,L] in 31 cases (94%); (2) TGA with solitus atria (S), L-loop ventricles (L), and D-TGA (D), that is, TGA [S,L,D] in 1 case (3%); and (3) TGA with inverted atria (I), D-loop ventricles (D), and D-TGA (D), that is, TGA [I,D,D] in 1 case (3%). Associated malformations resulted in 13 anatomic subtypes. In classical corrected TGA [S,L,L] with two ventricles, anomalies of the left-sided systemic tricuspid valve were present in 97%, with malformations of the left-sided systemic right ventricle in 91%. CONCLUSIONS: The findings in corrected TGA with two ventricles and in cases with single ventricle support the view that anatomic repair such as the double-switch procedure, or left-sided right ventricle bypass such as the modified Norwood procedure followed by the modified Fontan procedure, is indicated in selected patients.

Adolescent↗

[Pathologic karyotypes in autopsy material].

In 1986-1989 the authors were concerned with the cultivation of necroptic material. Material was collected from five indication groups outlined in advance. A total of 231 specimens of necroptic material were cultivated, incl. 143 specimens subjected to cytological evaluation. From the above material 20 pathological karyotypes were diagnosed. The results of cytogenetic analysis of chromosome abnormalities were compared with the clinical and pathological diagnosis. Post-mortem chromosome analysis is important for elucidation of the aetiopathogenesis of perinatal deaths and for a comprehensive approach to families with genetic risk.

Autopsy↗

[Postmortem chromosome analysis and its significance].

Cultivation of necroptic material taken by pathologist or obstetrician according to determined indicative groups was performed during the years 1986-1990. Cytogenetical evaluation was feasible in 157 cultivated samples from the total of 252. There were found 32 pathological karyotypes among them.

Abortion, Habitual↗

[Experience with postmortem chromosome analysis].

Over the years 1986-1988 necroptic material, collected according to 5 established indication groups, was cultured. A total of 202 samples of necroptic material cultured and 122 of these samples were analyzed cytogenetically. Seventeen pathologic karyotypes were diagnosed in the material, namely 7 cases of Down's syndrome, 2 cases of Klinefelter's syndrome, 2 cases of D/D translocation, 1 case of Turner's syndrome, 1 case of gonosomal mosaicism, and 1 case of Patau's syndrome.

Autopsy↗