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1.
Head Neck Pathol ; 4(4): 276-80, 2010 Dec.
Article in English | MEDLINE | ID: mdl-20857246

ABSTRACT

In this series, laryngeal preneoplastic lesions were evaluated by the classifications of the World Health Organization (WHOC), Ljubljana (LC) and squamous intraepithelial neoplasia (SINC) by multiple observers. The inter-observer agreement (IA) by WHOC for laryngeal lesions had been previously evaluated, but to the best of our knowledge, there are no data for LC and SINC. H&E stained slides from 42 laryngeal biopsies were evaluated by fourteen participants according to WHOC and LC, and SINC was additionally applied by 6. The results were analyzed statistically. The diagnoses which were favored by most participants for each case, according to WHOC, were as follows: squamous cell hyperplasia (n = 5; 12%), mild dysplasia (n = 11; 26.2%), moderate dysplasia (n = 12; 28.6%), severe dysplasia (n = 7; 16.7%), carcinoma in situ (n = 5; 12%), and invasive squamous cell carcinoma (n = 2; 4.8%). There was a significant difference between the participants for all three classifications; some participants gave lower or higher scores than the others. The mean correlation coefficients (MCC) of the participants were higher for WHOC compared to LC (0.55 ± 0.15 and 0.48 ± 0.14, respectively). The mean linear-weighted kappa (wKappa) values of participants were not significantly different (0.42 ± 0.10, 0.41 ± 0.12 and 0.37 ± 0.07 for WHOC, LC and SINC, respectively). The kappa values in this series are in agreement with those in previous literature for WHOC, and the similar results obtained for LC and SINC are novel findings. Although the MCC of WHOC was higher, as the wkappa was not significantly different, the findings in this series are not in favor of any of the classifications for better IA for pre-neoplastic laryngeal lesions.


Subject(s)
Biopsy/statistics & numerical data , Carcinoma, Squamous Cell/pathology , Laryngeal Neoplasms/pathology , Pathology, Clinical/statistics & numerical data , Precancerous Conditions/pathology , Biopsy/standards , Carcinoma in Situ/classification , Carcinoma in Situ/pathology , Carcinoma, Squamous Cell/classification , Humans , Laryngeal Neoplasms/classification , Observer Variation , Pathology, Clinical/standards , Precancerous Conditions/classification , World Health Organization
3.
Anal Quant Cytol Histol ; 30(5): 291-6, 2008 Oct.
Article in English | MEDLINE | ID: mdl-18980161

ABSTRACT

OBJECTIVE: To investigate the expression and distribution pattern of type IV collagen in dysplastic nevi (DN) and to determine whether DN exhibits a morphologic difference from common melanocytic nevi (CMN) and cutaneous malignant melanomas (MM) and therefore can be classified as a separate entity. STUDY DESIGN: We examined 33 DN specimens, 18 CMN specimens, and 10 MM specimens. The streptavidinbiotin immunoperoxidase method was used for immunostaining. RESULTS: No staining was observed in most of the CMN. Twenty-one of 33 DN showed a continuous pattern of type IV collagen surrounding junctional nests in a concentric fashion while a discontinuous immunostaining pattern was observed in remaining cases. Six of 10 MM showed a continuous staining pattern; 2 exhibited discontinuous staining; and in 2 cases, no immunostaining was observed. The expression pattern of type IV collagen in DN was statistically different from CMN and MM. CONCLUSION: Our results suggest sporadic DN is biologically different from CMN in terms of the capacity to synthesize type IV collagen, demonstrating that DN is not only morphologically but also biologically a different entity from CMN.


Subject(s)
Collagen Type IV/metabolism , Dysplastic Nevus Syndrome/metabolism , Dysplastic Nevus Syndrome/pathology , Skin Neoplasms/metabolism , Skin Neoplasms/pathology , Adolescent , Adult , Aged , Aged, 80 and over , Biomarkers, Tumor/metabolism , Biopsy , Child , Child, Preschool , Diagnosis, Differential , Humans , Immunoenzyme Techniques , Melanoma/metabolism , Melanoma/pathology , Middle Aged , Nevus, Pigmented/metabolism , Nevus, Pigmented/pathology , Staining and Labeling
4.
J Dtsch Dermatol Ges ; 6(2): 130-2, 2008 Feb.
Article in English, German | MEDLINE | ID: mdl-18076662

ABSTRACT

Although basal cell carcinoma is extremely common, it only rarely occurs on the nipple. Men are affected more often than women. Basal cell carcinoma of the nipple-areola complex may be more aggressive as metastases to regional lymph nodes have been reported. We report a basal cell carcinoma of the nipple with features of a fibroepithelioma of Pinkus in a man and review the literature.


Subject(s)
Breast Neoplasms, Male/diagnosis , Carcinoma, Basal Cell/diagnosis , Nipples , Skin Neoplasms/diagnosis , Biopsy , Breast Neoplasms, Male/pathology , Breast Neoplasms, Male/surgery , Carcinoma, Basal Cell/pathology , Carcinoma, Basal Cell/surgery , Diagnosis, Differential , Humans , Male , Mammography , Mastectomy, Simple , Middle Aged , Nipples/pathology , Nipples/surgery , Skin Neoplasms/pathology , Skin Neoplasms/surgery , Ultrasonography, Mammary
5.
J Diabetes Complications ; 21(5): 335-7, 2007.
Article in English | MEDLINE | ID: mdl-17825759

ABSTRACT

Amelanotic melanoma often leads to delayed clinical diagnosis because of its wide range of clinical appearances and lack of pigmentation. Misdiagnosis of amelanotic melanoma is also common, particularly when it is located at the foot. We report here a 71-year-old male patient with a 17-year history of type 2 diabetes mellitus who presented with a small ulcer under his fifth metatarsal head, which was previously misdiagnosed as a diabetic foot ulcer. The patient was treated with local wound care and systemic antibiotics without any improvement of the ulcer. Further investigation of the patient in our clinic revealed plantar amelanotic melanoma.


Subject(s)
Diabetic Foot/diagnosis , Melanoma, Amelanotic/diagnosis , Skin Neoplasms/diagnosis , Aged , Diabetic Angiopathies/diagnosis , Diabetic Foot/pathology , Diagnostic Errors , Glycated Hemoglobin/metabolism , Humans , Male , Melanoma, Amelanotic/pathology , Skin Neoplasms/pathology
6.
Urol Oncol ; 25(4): 326-8, 2007.
Article in English | MEDLINE | ID: mdl-17628300

ABSTRACT

A combination of some specific skin tumors with visceral cancers characterize Muir-Torre syndrome. A 60-year-old male patient who presented with penile keratoacanthoma accompanied by bladder and colorectal cancer is presented.


Subject(s)
Carcinoma, Transitional Cell/pathology , Keratoacanthoma/pathology , Neoplasms, Multiple Primary/pathology , Penile Diseases/pathology , Sebaceous Gland Neoplasms/pathology , Skin Neoplasms/pathology , Urinary Bladder Neoplasms/pathology , Humans , Keratoacanthoma/surgery , Male , Middle Aged , Penile Diseases/surgery , Syndrome
7.
Appl Immunohistochem Mol Morphol ; 15(2): 160-4, 2007 Jun.
Article in English | MEDLINE | ID: mdl-17525627

ABSTRACT

Familial acquired dysplastic nevi carry a risk for the development of melanoma. However, the results in various studies regarding the significance of sporadic dysplastic nevi as a precursor of malignant melanoma (MM), are controversial. The aim of this study is to investigate cyclin D1 expression and Ki67 proliferative index in a group of melanocytic lesions to address the biologic significance of sporadic dysplastic nevi in the progression of melanocytic lesions. Formalin-fixed paraffin-embedded material from 21 common melanocytic nevi, 42 dysplastic nevi, and 17 primary cutaneous MMs were examined. Standard streptavidin-biotin immunoperoxidase method was used for immunostaining with cyclin D1 and Ki-67 antibody. Nuclear cyclin D1 immunostaining was scored and Ki-67 proliferative index was calculated. Cyclin D1 expression was significantly higher in melanoma than those in other lesions. However, there was no significant difference between dysplastic nevi and common melanocytic nevi in terms of cyclin D1 expression. Ki-67 index was significantly higher in dysplastic nevi compared with common melanocytic nevi and to melanoma compared with dysplastic nevi. There was a significant positive correlation between cyclin D1 expression and Ki-67 proliferative index for each group. The present study indicates significant differences in cyclin D1 expressions and Ki-67 indices among melanocytic lesions. We think that dysplastic nevi are biologically separate from common melanocytic nevi in terms of proliferative activity. Additionally, our results suggest that cyclin D1 expression may be related to malignant phenotype and is associated with high proliferation rate in MM.


Subject(s)
Biomarkers, Tumor/metabolism , Cyclin D1/metabolism , Dysplastic Nevus Syndrome/metabolism , Ki-67 Antigen/metabolism , Melanoma/metabolism , Nevus, Pigmented/metabolism , Cyclin D1/genetics , Dysplastic Nevus Syndrome/pathology , Humans , Immunohistochemistry , Melanoma/pathology , Nevus, Pigmented/pathology
9.
Turk J Pediatr ; 48(2): 155-8, 2006.
Article in English | MEDLINE | ID: mdl-16848118

ABSTRACT

A three-year-old girl with a lingual plexiform neurofibroma treated by total excision is presented. Despite their occurrence in the head and neck region, neural sheath tumors are rarely encountered in the oral cavity. It is reported that 4-7% of patients affected by neurofibromatosis display oral manifestations. Neurofibromatosis is characterized by café-au-lait spots and cutaneous neurofibromas. Plexiform neurofibroma is said to be indicative of von Recklinghausen's disease (VRD) even though it may be the only manifestation of the disease. Generally, surgical resection represents the treatment of choice and the diagnosis can only be confirmed after histological examination. Affected patients need regular follow-up to detect malignant degeneration, an early recurrence or appearance of other manifestations of VRD.


Subject(s)
Neurofibroma, Plexiform/pathology , Tongue Neoplasms/pathology , Cafe-au-Lait Spots/etiology , Child, Preschool , Diagnosis, Differential , Female , Humans , Neurilemmoma/pathology , Neurofibroma, Plexiform/complications , Neurofibroma, Plexiform/surgery , Neurofibromatosis 1/pathology , Tongue Neoplasms/surgery
10.
Eur J Dermatol ; 16(2): 146-50, 2006.
Article in English | MEDLINE | ID: mdl-16581565

ABSTRACT

Although papulopustular lesions are common in patients with Behçet's disease (BD), clinically they may not be differentiated from other diseases with papulopustular presentation such as acne vulgaris or folliculitis. Therefore, there is disagreement as to whether they should be used as a diagnostic criterion in BD. The aim of this study was to determine whether the histopathologic evaluation of the papulopustular lesions may assist in the diagnosis of BD. Eighteen patients with BD and 16 control patients consisting of eleven patients with bacterial folliculitis and five patients with acne vulgaris were included in the study. After the detailed histopathologic evaluation by two pathologists who were blinded to the clinical diagnoses, the histopathologic findings were classified into three patterns as follows; pattern I: vasculitis (lymphocytic or leucocytoclastic); pattern II: folliculitis and/or perifolliculitis; pattern III: superficial and/or deep perivascular, and/or interstitial dermatitis. In addition, direct immunofluorescence studies were performed in order to evaluate the deposition of IgM, IgG, IgA, C3, or fibrinogen in dermal blood vessels. 27.8% of the patients with BD (5 patients) revealed lymphocytic vasculitis, while none of the control group did; and the difference was found statistically significant (P=0.046). The rate of pattern II which included folliculitis and/or perifolliculitis was 50.0% in control patients and 16.7% in the patients with BD; and the difference was found statistically significant (P=0.038). No difference was found between the two groups with regard to pattern III or direct immunofluorescence findings (P>0.05). Our results indicate that only vasculitic changes can be useful when histopathological features of papulopustular lesions are to be employed as a diagnostic criterion in patients with suspected BD.


Subject(s)
Behcet Syndrome/complications , Behcet Syndrome/pathology , Fluorescent Antibody Technique, Direct , Skin Diseases, Vesiculobullous/etiology , Skin Diseases, Vesiculobullous/pathology , Adult , Female , Humans , Male , Middle Aged
12.
Pathol Res Pract ; 201(5): 363-8, 2005.
Article in English | MEDLINE | ID: mdl-16047945

ABSTRACT

Oxalosis (calcium oxalate deposition) is associated with various conditions, including aspergillosis. Some Aspergillus species produce oxalic acid, which reacts with blood or tissue calcium to precipitate calcium oxalate. Calcium oxalate crystals exhibit various shapes and are strongly birefringent. These occur in cytological specimens, as well as in tissues of patients with Aspergillus infection. Aspergillus species are hyaline septate moulds, and they can be accurately recognized in pathology specimens only if conidial heads (fruiting heads) are present. When these structures are not observed, detection of associated oxalosis in a mould infection supports the pathological diagnosis of aspergillosis. The presence of oxalosis is helpful when microbiological identification or immunohistological techniques for fungi are not available. Calcium oxalate crystals can induce cellular injury by several mechanisms, and there is increasing evidence that oxalosis-induced tissue damage may occasionally lead to a poor clinical outcome. This review discusses the diagnostic value and the potential clinical significance of oxalosis associated with aspergillosis.


Subject(s)
Aspergillosis/diagnosis , Aspergillus/metabolism , Calcium Oxalate/metabolism , Aspergillosis/metabolism , Aspergillosis/microbiology , Aspergillus/growth & development , Calcium Oxalate/chemistry , Crystallization , Humans
13.
Pathol Res Pract ; 200(3): 181-8, 2004.
Article in English | MEDLINE | ID: mdl-15200269

ABSTRACT

There is still controversy about the classification of laryngeal preneoplastic lesions. In this study, we compared the World Health Organization (WHO) and Ljubljana histological classifications with regard to laryngeal epithelial hyperplastic-dysplastic lesions in a single series to determine their relation to statistically significant criteria when the mechanisms of neoplastic progression are considered. Emphasis was put on p53 expression, proliferative activity, and angiogenesis. Fifty-four laryngeal biopsies with preneoplastic changes were re-evaluated and classified according to both classifications. The streptavidin-biotin method was used for immunohistochemical staining for Ki-67, p53, and CD34 antibodies. A positive correlation was obtained between the histological categories and Ki-67, p53, and CD34 expressions using both classifications (Spearman's Correlation test). There was a significant difference between the histological categories of both the WHO and the Ljubljana classifications, when the expression of the three markers was compared (Kruskal Wallis test, p = 0.000 for each). Further evaluation revealed a statistically significant difference between all categories of both classifications, excluding the p53 overexpression scores and vessel counts in mild and moderate dysplasia categories (Mann-Whitney U-test, p = 0.209, and 0.091 respectively), and the p53 overexpression scores in severe dysplasia and carcinoma in situ categories (Mann-Whitney U-test, p = 0.249) of the WHO classification. Similarly, no significant differences were found between severe dysplasia and carcinoma in situ, as well as between atypical hyperplasia and carcinoma in situ categories using both classifications for the Ki-67 expression (Mann-Whitney U-test, p = 0.806, and 0.111, respectively). Our results suggest that regarding the mechanisms of neoplastic progression such as p53 expression and angiogenesis, the histological categories of the Ljubljana classification seem to depend on additional evidence. Therefore, we support the use of the Ljubljana classification.


Subject(s)
Laryngeal Mucosa/pathology , Laryngeal Neoplasms/diagnosis , Precancerous Conditions/diagnosis , World Health Organization , Adenocarcinoma/classification , Adenocarcinoma/diagnosis , Adenocarcinoma/metabolism , Adult , Aged , Antigens, CD34/metabolism , Biomarkers, Tumor/metabolism , Carcinoma in Situ/classification , Carcinoma in Situ/diagnosis , Carcinoma in Situ/metabolism , Female , Humans , Hyperplasia/classification , Hyperplasia/diagnosis , Hyperplasia/metabolism , Immunohistochemistry , Ki-67 Antigen/metabolism , Laryngeal Mucosa/metabolism , Laryngeal Neoplasms/classification , Laryngeal Neoplasms/metabolism , Male , Middle Aged , Precancerous Conditions/classification , Precancerous Conditions/metabolism , Tumor Suppressor Protein p53/metabolism
14.
Ear Nose Throat J ; 83(5): 331-3, 2004 May.
Article in English | MEDLINE | ID: mdl-15195880

ABSTRACT

We report a case of isolated nasopharyngeal aspergillosis in a 52-year-old woman with Hashimoto's thyroiditis. We found the nasopharyngeal lesion incidentally while evaluating bilateral cervical lymphadenopathy, which we had discovered during a routine follow-up examination pursuant to the patient's thyroid problem. Biopsy analysis of the nasopharyngeal lesion revealed the presence of a mycelium made up of septate hyphae and associated oxalosis. Mycologic examination confirmed that Aspergillus flavus was the responsible pathogen. No systemic involvement or involvement of other head and neck sites was found. The patient had been exposed to a considerable amount of dust during the construction of her house, and this may have been the precipitating factor in the development of her infection. We treated the patient with a 4-week course of itraconazole. At the end of therapy, she exhibited no evidence of A flavus on physical and mycologic examinations.


Subject(s)
Aspergillosis/diagnosis , Aspergillus flavus/isolation & purification , Calcium Oxalate/metabolism , Nasopharyngeal Diseases/diagnosis , Nasopharynx/microbiology , Antifungal Agents/therapeutic use , Aspergillosis/drug therapy , Aspergillosis/metabolism , Aspergillosis/microbiology , Female , Humans , Itraconazole/therapeutic use , Middle Aged , Nasopharyngeal Diseases/drug therapy , Nasopharyngeal Diseases/metabolism , Nasopharyngeal Diseases/microbiology , Nasopharynx/metabolism , Nasopharynx/pathology , Thyroiditis, Autoimmune/complications
16.
Pathol Res Pract ; 198(10): 675-8, 2002.
Article in English | MEDLINE | ID: mdl-12498222

ABSTRACT

Candidiasis of the larynx is rare, and candidal involvement of the larynx mostly occurs after pulmonary, pharyngeal and esophageal candidiasis, or as part of disseminated disease. We here report our morphologic observations made in five cases of laryngeal candidiasis. These cases had the following morphologic features in common: 1. pronounced epithelial hyperplasia, which may show a verrucous pattern, 2. prominent ortho-parakeratosis, and 3. predominantly neutrophilic infiltration located in the upper layers of the mucosal epithelium. Our morphologic observations were similar to the morphologic changes encountered in chronic hyperplastic candidosis of the oral mucosa. As this type of candidal lesions contains fewer hyphae than the usual thrush, fungal infection may be easily overlooked. Pronounced epithelial hyperplasia and prominent ortho-parakeratosis may mimic squamous cell and verrucous carcinomas. In conclusion, we suggest performing special stains for fungi of laryngeal biopsies that have the morphologic features mentioned above. In that way, it is possible to detect a candidal infection, keeping in mind that the fungal organisms may be very few in number and morphologically distorted.


Subject(s)
Candidiasis/pathology , Diagnostic Errors/prevention & control , Laryngeal Diseases/pathology , Larynx/pathology , Adult , Female , Humans , Hyperplasia , Laryngeal Diseases/microbiology , Larynx/microbiology , Male , Middle Aged , Periodic Acid-Schiff Reaction
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