scholarly journals Habit tic nail dystrophy: a case report affecting single thumb nail

2020 ◽  
Vol 8 (8) ◽  
pp. 3083
Author(s):  
Boby John Oommen ◽  
Waad Ibrahim Majed Kadori
Keyword(s):  
Case Report ◽  
Nail Dystrophy ◽  
Simple Treatment ◽  
Treatment Measure

Habit-tic deformity is a classic example of overlap between the domains of dermatology and psychiatry.  Mostly seen in adults, it results from the habit of picking or pushing the cuticle backward. A case of habit-tic deformity of a single thumb nail is reported and the simple treatment measure adopted discussed.

scholarly journals Oral and Dental Changes of Dyskeratosis Congenita: A Case Report with Literature Review

2018 ◽  
Vol 9 (1-2) ◽  
pp. 20-23 ◽  
Author(s):  
Gozde Serindere
Keyword(s):  
Case Report ◽  
Early Diagnosis ◽  
Literature Review ◽  
Aggressive Periodontitis ◽  
Dyskeratosis Congenita ◽  
Tooth Decay ◽  
Nail Dystrophy ◽  
Uncommon Disease ◽  
Missing Tooth ◽  
Enamel Layer

Dyskeratosis congenita (DC) is an uncommon disease characterized by nail dystrophy, cutaneous hyperpigmentation, leukoplakia, pancytopenia, and malignant transformation. There can be some oral and dental changes such as oral leukoplakia, increase in tooth decay, hypodontia, thinning of enamel layer, aggressive periodontitis, intraoral brown pigmentation, missing tooth, taurodontism, and blunted roots. Most of cases belong to dermatology or pediatrics department. There are few reports about dentistry. The aim of this report is to lay emphasis on this fatal syndrome among dentists about the multisystem findings and oro-dental changes. Thus, this information may aid dentists in early diagnosis. A case of 21-year-old male diagnosed with DC is reported.

Facial and bilateral acral porokeratosis with nail dystrophy: A case report

2011 ◽  
Vol 17 (1) ◽  
Author(s):  
Reza Mahmoud Robati ◽  
Mohammad Rahmati-Roodsari ◽  
Azin Ayatollahi ◽  
Somaye Hejazi
Keyword(s):  
Case Report ◽  
Nail Dystrophy

scholarly journals Inherited Epidermolysis Bullosa – A Case Report of Several Family Members in Three Generations

2018 ◽  
Vol 10 (1) ◽  
pp. 12-17
Author(s):  
Ljuba Vujanović ◽  
Marina Jovanović ◽  
Zoran Golušin ◽  
Svetlana Kovačić Dukić ◽  
Sanja Jakovljević ◽  
...  
Keyword(s):  
Case Report ◽  
Female Patient ◽  
Epidermolysis Bullosa ◽  
Autosomal Dominant ◽  
Dorsal Plate ◽  
Nail Dystrophy ◽  
Three Generations ◽  
The Family ◽  
Inherited Epidermolysis Bullosa ◽  
Atrophic Scars

Abstract Inherited epidermolysis bullosa (IEB) is a genodermatosis transmitted in either autosomal dominant or autosomal recessive manner. The disease is characterized by the development of blisters, erosions, scars, nail dystrophy and scalp abnormalities. Our case report has included four members of one family in three generations with manifested disease. Our 25-year-old female patient presented with a few eroded, crusted, nummular lesions localized on the dorsal plate of interphalangeal joints of fingers, elbow and knee skin, while anonychia was found on her digits. Our youngest patient (her 3.5-year-old son) presented with the lesions in the form of blisters filled with serous fluid, erosions, recent scars and atrophy. Some atrophic scars on the elbow and knee skin were found in our patient′s younger brother, aged 16. The 46-year-old mother of our female patient had nail dystrophy on her hands accompanied by the toenails absence. Pediatric geneticist created the pedigree chart which showed autosomal dominant inheritance pattern with complete expressivity and penetrance. Further diagnostics was not done because the family was not interested.

A Single Nail Dystrophy as a Unique Manifestation of Sarcoidosis: A Case Report

2021 ◽  
pp. 1-4
Author(s):  
Laura Mengeot ◽  
Bernard Stallenberg ◽  
Ivan Théate ◽  
Oliver Vanhooteghem
Keyword(s):  
Case Report ◽  
Clinical Evaluation ◽  
Systemic Disease ◽  
Radiological Examination ◽  
Bone Involvement ◽  
Nail Dystrophy ◽  
Nail Changes ◽  
Osseous Involvement ◽  
Nail Involvement

Sarcoidosis with nail involvement is rare and most commonly affecting plural digits. Nail changes are frequently an indication of systemic disease and underlying bone involvement, thus complete clinical evaluation with bone and thorax radiological examination is a necessity in suspected cases. We report a case of onychodystrophy with osseous involvement of only one finger as unique manifestation of sarcoidosis, which is very rare.

A Simple Treatment for a 15-cm Tibia Bone Defect: A Case Report of an Ipsilateral Vascularized Fibula Transfer

2007 ◽  
Vol 21 (3) ◽  
pp. 215-218 ◽  
Author(s):  
Panagiotis Koulouvaris ◽  
Christos Theos ◽  
Stamatis Kottakis ◽  
Nikolaos Demertzis
Keyword(s):  
Case Report ◽  
Bone Defect ◽  
Simple Treatment ◽  
Tibia Bone ◽  
Vascularized Fibula

scholarly journals Acute Felon as a Complication of Systemic Paclitaxel Therapy: Case Report and Review of the Literature

Hand ◽  
2007 ◽  
Vol 2 (3) ◽  
pp. 101-103 ◽  
Author(s):  
John B. Hijjawi ◽  
David G. Dennison
Keyword(s):  
Breast Cancer ◽  
Case Report ◽  
Cancer Patient ◽  
Breast Cancer Patient ◽  
Upper Extremity ◽  
Unusual Case ◽  
Review Of The Literature ◽  
Nail Dystrophy ◽  
American Women ◽  
History Of

Breast cancer now affects 1 in 8 American women and the taxane agent paclitaxel (Taxol® Bristol-Myers Squibb) is a major tool in the treatment of many such patients. Hand surgeons are therefore likely to encounter upper extremity complications related to the use of taxane therapy. We present an unusual case of a felon developing in a breast cancer patient on paclitaxel therapy with no antecedent history of trauma. Whereas onycholysis and subungual hemorrhage are reported complications of taxane therapy ( Fig. 1 ), an acute felon with or without associated paronychia is an unusual and more aggressive manifestation of this drug-related nail dystrophy.

scholarly journals Dyskeratosis congenita: a rare case report

2013 ◽  
Vol 33 (3) ◽  
pp. 223-226 ◽  
Author(s):  
Banasree Roy ◽  
Gobinda Mondal ◽  
Dilip Kumar Paul ◽  
Abul Kalam ◽  
Kausambi Basu
Keyword(s):  
Bone Marrow ◽  
Case Report ◽  
Rare Case ◽  
Progressive Disease ◽  
Dyskeratosis Congenita ◽  
Congenital Disorder ◽  
Nail Dystrophy ◽  
Rare Congenital Disorder ◽  
Rare Case Report

Dyskeratosis congenita is a rare congenital disorder affecting mainly the integumentary system. It is a progressive disease with involvement of bone marrow. A triad of hyperpigmentation, nail dystrophy and leucoplakia are characteristic of this disease. DOI: http://dx.doi.org/10.3126/jnps.v33i3.8166   J. Nepal Paediatr. Soc. 2013;33(3):223-226

A case report of rare palmoplantar keratosis and nail dystrophy with imatinib

2017 ◽  
Vol 75 (3) ◽  
pp. 172-175 ◽  
Author(s):  
M. Benabbes ◽  
Z. Tazi Mezalek ◽  
B. Meddah
Keyword(s):  
Case Report ◽  
Nail Dystrophy ◽  
Palmoplantar Keratosis
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