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1.
Am J Dermatopathol ; 44(9): 658-663, 2022 Sep 01.
Article in English | MEDLINE | ID: mdl-35503878

ABSTRACT

ABSTRACT: Oral pigmentations are a heterogeneous group and can be the result of physiological activity of oral mucosal melanocytes, secondary to exogenous causes, associated with systemic or local diseases, or due to proliferative activity of melanocytes. Their diagnosis is critical because these lesions can be markers of internal diseases or, in the case of melanocytic proliferative processes, they may represent a malignant neoplasm. In the past decade, the use of reflectance confocal microscopy, a noninvasive imaging tool, has aided the analysis of such lesions, but the establishment of firm criteria in their evaluation is still lacking. This study evaluated a series of 19 cases of pigmented oral lesions and correlated the reflectance confocal microscopy findings with histopathological classical criteria. We found 13 cases of melanotic macule, 1 of them associated with Peutz-Jeghers syndrome and 2 with Laugier-Hunzinker syndrome; 1 melanocytic nevus; 2 lentigo maligna; 2 pigmented actinic cheilitis; and 1 case of postinflammatory pigmentation secondary to a lupus erythematosus oral discoid lesion. The main difference between benign and malignant lesions was the presence of atypical proliferation in lentigo maligna. Langerhans cells with thick dendritic processes, which may be present in other benign and inflammatory pigmentations is one of the main reasons for diagnostic pitfalls.


Subject(s)
Hutchinson's Melanotic Freckle , Nevus, Pigmented , Pigmentation Disorders , Skin Neoplasms , Diagnosis, Differential , Humans , Hutchinson's Melanotic Freckle/pathology , Melanocytes/pathology , Microscopy, Confocal/methods , Nevus, Pigmented/pathology , Pigmentation Disorders/diagnostic imaging , Skin Neoplasms/pathology
2.
J Healthc Eng ; 2018: 9397105, 2018.
Article in English | MEDLINE | ID: mdl-30651950

ABSTRACT

Diabetic skin manifestations, previous to ulcers and wounds, are not highly accounted as part of diagnosis even when they represent the first symptom of vascular damage and are present in up to 70% of patients with diabetes mellitus type II. Here, an application for skin macules characterization based on a three-stage segmentation and characterization algorithm used to classify vascular, petechiae, trophic changes, and trauma macules from digital photographs of the lower limbs is presented. First, in order to find the skin region, a logical multiplication is performed on two skin masks obtained from color space transformations; dynamic thresholds are stabilised to self-adjust to a variety of skin tones. Then, in order to locate the lesion region, illumination enhancement is performed using a chromatic model color space, followed by a principal component analysis gray-scale transformation. Finally, characteristics of each type of macule are considered and classified; morphologic properties (area, axes, perimeter, and solidity), intensity properties, and a set of shade indices (red, green, blue, and brown) are proposed as a measure to obviate skin color differences among subjects. The values calculated show differences between macules with a statistical significance, which agree with the physician's diagnosis. Later, macule properties are fed to an artificial neural network classifier, which proved a 97.5% accuracy, to differentiate between them. Characterization is useful in order to track macule changes and development along time, provides meaningful information to provide early treatments, and offers support in the prevention of amputations due to diabetic feet. A graphical user interface was designed to show the properties of the macules; this application could be the background of a future Diagnosis Assistance Tool for educational (i.e., untrained physicians) and preventive assistance technology purposes.


Subject(s)
Diabetes Complications/diagnostic imaging , Diabetes Mellitus, Type 2/complications , Image Processing, Computer-Assisted/methods , Leg/diagnostic imaging , Pigmentation Disorders/diagnostic imaging , Skin/diagnostic imaging , Algorithms , Color , Computer Graphics , Diabetes Complications/pathology , Diabetes Mellitus, Type 2/diagnostic imaging , Diabetic Foot/complications , Humans , Leg/pathology , Neural Networks, Computer , Photography , Pigmentation Disorders/pathology , Principal Component Analysis , Purpura/pathology , Skin/pathology , Skin Abnormalities/diagnostic imaging , Skin Pigmentation , Software , User-Computer Interface
3.
Rev. bras. oftalmol ; 76(6): 312-315, nov.-dez. 2017. graf
Article in English | LILACS | ID: biblio-899098

ABSTRACT

Abstract We report a case of a middle-aged woman who developed acute, bilateral, symmetrical, slightly transilluminating depigmentation of the iris and pigment discharge into the anterior chamber following the use of oral moxifloxacin for bacterial sinusitis. She had been misdiagnosed as having autoimmune uveitis, treated with steroids and tropicamide, and underwent severe ocular hypertension and glaucoma despite posterior correct diagnosis.


Resumo Relato de um caso de uma paciente do sexo feminino de meia idade que desenvolveu despigmentação bilateral simultânea aguda com dispersão de pigmentos na câmara anterior e discreta transiluminação após o uso de moxifloxacino oral para tratamento de sinusite bacteriana. Ela Havia sido diagnosticada com uveite autoimune e tratada com corticosteroide tópico e tropicamida e evoluiu com hipertensão ocular grave e glaucoma apesar de ,posteriormente, o diagnóstico ter sido correto.


Subject(s)
Humans , Female , Adult , Glaucoma/etiology , Ocular Hypertension/etiology , Iris Diseases/complications , Pigment Epithelium of Eye/diagnostic imaging , Pigmentation Disorders/diagnostic imaging , Trabecular Meshwork/pathology , Transillumination , Iridocyclitis/diagnosis , Glaucoma/drug therapy , Glaucoma/diagnostic imaging , Iris/diagnostic imaging , Ocular Hypertension/drug therapy , Ocular Hypertension/diagnostic imaging , Acute Disease , Photophobia , Tomography, Optical Coherence , Visual Field Tests , Brimonidine Tartrate/administration & dosage , Slit Lamp Microscopy , Moxifloxacin/adverse effects , Gonioscopy , Iris Diseases/chemically induced , Iris Diseases/diagnostic imaging , Anterior Chamber/pathology , Antihypertensive Agents/administration & dosage
4.
An. bras. dermatol ; An. bras. dermatol;91(6): 764-769, Nov.-Dec. 2016. tab, graf
Article in English | LILACS | ID: biblio-837998

ABSTRACT

Abstract BACKGROUND: Dermatoscopy is a non-invasive diagnostic tool used to examine skin lesions with an optical magnification. It has been suggested as a useful tool for monitoring therapeutic response in lentigo maligna patients treated with imiquimod. OBJECTIVE: To examine the accuracy of dermatoscopy as a tool to monitor the therapeutic response of pigmented basal cell carcinoma treated with imiquimod. METHOD: The authors designed a prospective study. Patients with pigmented basal cell carcinoma were included and data regarding the dermatoscopy features were collected following the Menzies criteria, prior to initiating the imiquimod treatment. Subsequent dermatoscopic evaluations were performed at weeks 4 and 8, following imiquimod discontinuation. RESULTS: Twenty lesions were included. The most common pigmented dermatoscopy features were large blue-grey ovoid nests (80%), followed by blue-grey globules (50%) and leaf-like areas (30%). No spoke wheel areas were observed. In 17 out of 20 patients, a response was noted during the first evaluation at 4 weeks, while the clearance was noted at the second check-up after 8 weeks. In two patients, the clearance was found at the initial evaluation at 4 weeks, while in one patient, the response remained unchanged. Blue-grey globules were the fastest to exhibit clearance (50% at week 4), followed by leaf-like areas (15%) and large blue-grey ovoid nests (6.25%). CONCLUSION: According to our results, dermatoscopic evaluation enhances the accuracy in the assessment of the clinical response to imiquimod in pigmented basal cell carcinoma.


Subject(s)
Humans , Male , Female , Middle Aged , Aged , Aged, 80 and over , Skin Neoplasms/diagnostic imaging , Carcinoma, Basal Cell/drug therapy , Carcinoma, Basal Cell/diagnostic imaging , Dermoscopy/methods , Aminoquinolines/therapeutic use , Antineoplastic Agents/therapeutic use , Pigmentation Disorders/pathology , Pigmentation Disorders/drug therapy , Pigmentation Disorders/diagnostic imaging , Skin/pathology , Skin Neoplasms/pathology , Time Factors , Carcinoma, Basal Cell/pathology , Prospective Studies , Reproducibility of Results , Treatment Outcome
5.
An Bras Dermatol ; 91(5): 584-587, 2016.
Article in English | MEDLINE | ID: mdl-27828629

ABSTRACT

BACKGROUND:: Pigmented purpuric dermatosis is a chronic skin disorder of unknown aetiology characterised by symmetrical petechial and pigmented macules, often confined to the lower limbs. The aetiology of pigmented purpuric dermatosis is unknown. Dermatoscopy is a non-invasive diagnostic technique that allows the visualisation of morphological features invisible to the naked eye; it combines a method that renders the corneal layer of the skin translucent with an optical system that magnifies the image projected onto the retina. OBJECTIVES:: The aim of this study is to investigate the dermatoscopic findings of pigmented purpuric dermatosis. METHODS:: This study enrolled patients diagnosed histopathologically with pigmented purpuric dermatosis who had dermatoscopic records. We reviewed the dermatoscopic images of PPD patients who attended the outpatient clinic in the Istanbul Dermatovenereology Department at the Bezmialem Vakif University Medical Faculty. RESULTS:: Dermatoscopy showed: coppery-red pigmentation (97%, n = 31) in the background, a brown network (34%, n = 11), linear vessels (22%, n = 7), round to oval red dots, globules, and patches (69%, n = 22; 75%, n = 24; 34%, n = 11; respectively), brown globules (26%, n = 8) and dots (53%, n = 17), linear brown lines (22%, n = 7), and follicular openings (13%, n = 4). CONCLUSION:: To our knowledge, this is the first study to report the dermatoscopy of pigmented purpuric dermatosis. In our opinion, dermatoscopy can be useful in the diagnosis of pigmented purpuric dermatosis.


Subject(s)
Dermoscopy/methods , Pigmentation Disorders/diagnostic imaging , Purpura/diagnostic imaging , Adolescent , Adult , Aged , Cholesterol, LDL/blood , Female , Humans , Male , Medical Records , Middle Aged , Pigmentation Disorders/pathology , Purpura/pathology , Young Adult
6.
An. bras. dermatol ; An. bras. dermatol;91(5): 584-587, Sept.-Oct. 2016. tab, graf
Article in English | LILACS | ID: biblio-827760

ABSTRACT

Abstract: Background: Pigmented purpuric dermatosis is a chronic skin disorder of unknown aetiology characterised by symmetrical petechial and pigmented macules, often confined to the lower limbs. The aetiology of pigmented purpuric dermatosis is unknown. Dermatoscopy is a non-invasive diagnostic technique that allows the visualisation of morphological features invisible to the naked eye; it combines a method that renders the corneal layer of the skin translucent with an optical system that magnifies the image projected onto the retina. Objectives: The aim of this study is to investigate the dermatoscopic findings of pigmented purpuric dermatosis. Methods: This study enrolled patients diagnosed histopathologically with pigmented purpuric dermatosis who had dermatoscopic records. We reviewed the dermatoscopic images of PPD patients who attended the outpatient clinic in the Istanbul Dermatovenereology Department at the Bezmialem Vakıf University Medical Faculty. Results: Dermatoscopy showed: coppery-red pigmentation (97%, n = 31) in the background, a brown network (34%, n = 11), linear vessels (22%, n = 7), round to oval red dots, globules, and patches (69%, n = 22; 75%, n = 24; 34%, n = 11; respectively), brown globules (26%, n = 8) and dots (53%, n = 17), linear brown lines (22%, n = 7), and follicular openings (13%, n = 4). Conclusion: To our knowledge, this is the first study to report the dermatoscopy of pigmented purpuric dermatosis. In our opinion, dermatoscopy can be useful in the diagnosis of pigmented purpuric dermatosis.


Subject(s)
Humans , Male , Female , Adolescent , Adult , Middle Aged , Aged , Young Adult , Pigmentation Disorders/diagnostic imaging , Purpura/diagnostic imaging , Dermoscopy/methods , Pigmentation Disorders/pathology , Purpura/pathology , Medical Records , Cholesterol, LDL/blood
7.
An Bras Dermatol ; 91(6): 764-769, 2016.
Article in English | MEDLINE | ID: mdl-28099598

ABSTRACT

BACKGROUND:: Dermatoscopy is a non-invasive diagnostic tool used to examine skin lesions with an optical magnification. It has been suggested as a useful tool for monitoring therapeutic response in lentigo maligna patients treated with imiquimod. OBJECTIVE:: To examine the accuracy of dermatoscopy as a tool to monitor the therapeutic response of pigmented basal cell carcinoma treated with imiquimod. METHOD:: The authors designed a prospective study. Patients with pigmented basal cell carcinoma were included and data regarding the dermatoscopy features were collected following the Menzies criteria, prior to initiating the imiquimod treatment. Subsequent dermatoscopic evaluations were performed at weeks 4 and 8, following imiquimod discontinuation. RESULTS:: Twenty lesions were included. The most common pigmented dermatoscopy features were large blue-grey ovoid nests (80%), followed by blue-grey globules (50%) and leaf-like areas (30%). No spoke wheel areas were observed. In 17 out of 20 patients, a response was noted during the first evaluation at 4 weeks, while the clearance was noted at the second check-up after 8 weeks. In two patients, the clearance was found at the initial evaluation at 4 weeks, while in one patient, the response remained unchanged. Blue-grey globules were the fastest to exhibit clearance (50% at week 4), followed by leaf-like areas (15%) and large blue-grey ovoid nests (6.25%). CONCLUSION:: According to our results, dermatoscopic evaluation enhances the accuracy in the assessment of the clinical response to imiquimod in pigmented basal cell carcinoma.


Subject(s)
Aminoquinolines/therapeutic use , Antineoplastic Agents/therapeutic use , Carcinoma, Basal Cell/diagnostic imaging , Carcinoma, Basal Cell/drug therapy , Dermoscopy/methods , Skin Neoplasms/diagnostic imaging , Skin Neoplasms/drug therapy , Aged , Aged, 80 and over , Carcinoma, Basal Cell/pathology , Female , Humans , Imiquimod , Male , Middle Aged , Pigmentation Disorders/diagnostic imaging , Pigmentation Disorders/drug therapy , Pigmentation Disorders/pathology , Prospective Studies , Reproducibility of Results , Skin/pathology , Skin Neoplasms/pathology , Time Factors , Treatment Outcome
8.
J Pediatr ; 115(1): 75-80, 1989 Jul.
Article in English | MEDLINE | ID: mdl-2738798

ABSTRACT

Nineteen children with hypomelanosis of Ito are described. Fourteen were developmentally delayed and nine had a history of seizures. Hemihypertrophy was present in four patients, syndactyly in three, and scoliosis in one. Twelve of the children had abnormal electroencephalograms and nine had abnormal brain scans, four with appearances suggestive of abnormal neuronal migration. There is very little evidence, either from the literature or from our patients, that the disease is inherited. The pattern of the cutaneous lesions suggests that the condition may result from the presence of two different cell populations as a result of mosaicism.


Subject(s)
Mosaicism , Pigmentation Disorders/genetics , Brain/diagnostic imaging , Child , Electroencephalography , Female , Genetic Linkage , Humans , Infant , Infant, Newborn , Male , Pigmentation Disorders/diagnostic imaging , Pigmentation Disorders/physiopathology , Radiography , X Chromosome
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