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1.
Eur J Histochem ; 52(4): 251-4, 2008.
Article in English | MEDLINE | ID: mdl-19109100

ABSTRACT

A case of hyalinizing clear cell carcinoma (HCCC) of the minor salivary glands of the oral cavity is reported. A 52- year-old woman presented with a growing mass at the base of the tongue. The patient underwent complete resection of the tumour. The histological picture was characterized by trabeculae or solid nests of proliferating cells with a clear cytoplasm, surrounded by a hyalinizing stroma. Tumour cells were immunoreactive for Cytokeratins 5, 6, 7, 8, 14, 17 and 18. No reactivity was observed for cytokeratin 20, vimentin, S- 100 protein, smooth-muscle actin, muscle-specific actin, and calponin. These findings confirmed the diagnosis of HCCC of minor salivary glands of the oral cavity. The clinical presentation, the immunohistochemical pattern and the role of cytokeratins in the differential diagnosis of HCCC are discussed with a review of the literature.


Subject(s)
Adenocarcinoma, Clear Cell/diagnosis , Immunohistochemistry/methods , Salivary Gland Neoplasms/diagnosis , Salivary Glands, Minor/pathology , Adenocarcinoma, Clear Cell/chemistry , Adenocarcinoma, Clear Cell/surgery , Adenoma, Oxyphilic/diagnosis , Biomarkers, Tumor/analysis , Carcinoma, Mucoepidermoid/diagnosis , Carcinoma, Renal Cell/diagnosis , Carcinoma, Renal Cell/secondary , Diagnosis, Differential , Female , Humans , Hyalin/metabolism , Keratins/analysis , Melanoma/diagnosis , Melanoma/secondary , Middle Aged , Myoepithelioma/diagnosis , Salivary Gland Neoplasms/chemistry , Salivary Gland Neoplasms/surgery , Salivary Glands, Minor/chemistry , Salivary Glands, Minor/surgery
2.
Cancer Genet Cytogenet ; 88(2): 158-62, 1996 Jun.
Article in English | MEDLINE | ID: mdl-8640727

ABSTRACT

Cytogenetic investigation on short-term cultures of 13 nasal polyps disclosed the presence of chromosome aberrations in three cases: one (a recurrence) showed numerical changes; the other two had structural abnormalities, an inv(12)(q15q22) in one case, a der(6)t(6;12)(q22;q15) in the other. The three cases were characterized histologically by the presence of frequent atypical stromal cells, and were positive for vimentin and smooth muscle actin. Of the remaining 10 cases, three were not analyzable, and seven had normal karyotypes, although random structural changes were seen in two of them.


Subject(s)
Chromosome Aberrations/genetics , Nasal Polyps/genetics , Adult , Aged , Child , Chromosome Disorders , Female , Humans , Karyotyping , Male , Middle Aged , Nasal Polyps/pathology , Stromal Cells/pathology
3.
Genes Chromosomes Cancer ; 10(3): 203-6, 1994 Jul.
Article in English | MEDLINE | ID: mdl-7522044

ABSTRACT

The etiology of nasal polyposis is not fully understood. We found numerical chromosome changes in one out of five cytogenetically investigated nasal polyps. The histological picture of this case was characterized by the presence of histiocyte-like cells, which were absent in the remaining cytogenetically normal polyps.


Subject(s)
Chromosome Aberrations , Nasal Polyps/genetics , Adult , Cells, Cultured , Child , Humans , Immunohistochemistry , Karyotyping , Male
4.
Minerva Anestesiol ; 58(5): 319-21, 1992 May.
Article in Italian | MEDLINE | ID: mdl-1635646

ABSTRACT

An intravenous anesthesia with propofol and fentanyl was used for adenotonsillectomy in a child affected by mucopolysaccharidosis. This technique proved to be safe and convenient without peri- and postoperative complications.


Subject(s)
Anesthesia, Intravenous , Fentanyl , Mucopolysaccharidosis III , Propofol , Tonsillectomy , Child, Preschool , Humans , Male
5.
Acta Otorhinolaryngol Ital ; 11(6): 595-601, 1991.
Article in Italian | MEDLINE | ID: mdl-1819187

ABSTRACT

This paper discusses the personal criteria followed in indicating tonsillectomy and/or adenotonsillectomy in treating a group of 150 children between the ages of 2 and 12 in the ENT Department of the Crobu Hospital of Iglesias where a follow-up was carried out from May 1989 to March 1991. The study analyzes when and under what conditions these surgical procedures are indicated in young patients without recurrent tonsillitis but with obstructive sleep apnea (OSA). The utility of traditional laboratory investigations (such as surface pharyngeal swabbing) in indicating surgical therapy is also evaluated. In concluding, the Authors affirm that recurrent tonsillitis no longer controllable with medical therapy is still the most frequent indication for surgery. In fact, 64% of the children studied belonged to either class TR or ITR in which recurring infection was the primary indication factor. However, respiratory obstruction has recently emerged as a increasingly important factor in indicating tonsillectomy and/or adenotonsillectomy. In fact, 54 children (35.9%) of the 150 studied belonged to class IT or OSA in which tonsillar and/or adeno-tonsillar hypertrophy with obstruction of various degrees was the determining factor in indicating surgical treatment. It appears that in the near future with fewer tonsillectomies being indicated in the case of recurrent tonsillitis, a progressive increase in the number of indications of surgical treatment in cases of obstruction may be expected. The Authors stress, however, the importance of identifying OSA patients because of the cardiorespiratory risks they may encounter during surgery (intubation difficulty found by the anaesthesiologist, tendency towards laryngeal spasms and pharyngeal obstruction in the post-operatory period).


Subject(s)
Tonsillectomy , Adenoidectomy , Child , Child, Preschool , Female , Humans , Male , Sleep Apnea Syndromes/surgery , Tonsillitis/surgery
6.
Blood ; 69(5): 1300-6, 1987 May.
Article in English | MEDLINE | ID: mdl-3567357

ABSTRACT

Mepacrine uptake into platelets and bone marrow megakaryocytes was analyzed to further characterize the dense granule defects in a group of seven mouse pigment mutants that have characteristics of platelet storage pool disease (SPD). In contrast to our previous studies using electron microscopy, this method revealed that all mutants had normal numbers of dense granules. However, total mepacrine uptake in all mutant platelets was significantly diminished to less than 50% of normal uptake. Also, the flashing phenomenon observed when normal dense granules are irradiated with ultraviolet light was either greatly diminished or absent when platelets of individual mutants were similarly irradiated. Therefore the principal defect in the mutant platelets is an inability to accumulate dense granule contents rather than an absence of the granules. Mepacrine uptake into megakaryocytes was indistinguishable in normal and mutant mice. This indicates the mutant dense granule defects appear either very late in megakaryocyte development or early in platelet formation in correlation with development of the mature dense granule. By standard transmission electron microscopy we have not been able to detect gross structural or subcellular abnormalities in either platelets or megakaryocytes of mutant mice. It appears all seven mutants produce immature or functionally abnormal dense granules.


Subject(s)
Blood Platelet Disorders/blood , Blood Platelets/ultrastructure , Cytoplasmic Granules/classification , Animals , Blood Platelets/metabolism , Cytoplasmic Granules/metabolism , Disease Models, Animal , Female , Male , Megakaryocytes/metabolism , Megakaryocytes/ultrastructure , Mice , Mice, Inbred Strains , Microscopy, Electron , Quinacrine/metabolism , Syndrome
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