scholarly journals Blistering in a newborn: a rare case report

2020 ◽  
Vol 6 (3) ◽  
pp. 432
Author(s):  
Jasleen Kaur ◽  
Jyoti Budhwar ◽  
Ankush Maheshwary ◽  
Karandeep Singh Bhatti
Keyword(s):  
Case Report ◽  
Physical Examination ◽  
Skin Biopsy ◽  
Epidermolysis Bullosa ◽  
Rare Case ◽  
Epidermolysis Bullosa Simplex ◽  
Lower Lip ◽  
Minimal Trauma ◽  
Rare Case Report ◽  
Female Baby

<p>Epidermolysis bullosa is a heterogeneous group of inherited mechanobullous disorders that present with skin and mucosal fragility, leading to blister formation after minimal trauma. 18 days old female baby presented with fluid-filled blisters of variable sizes over the lower lip, bilateral heels, hands, buttocks, chest, legs and arms, which ruptured spontaneously leaving raw areas. The history and physical examination suggested epidermolysis bullosa simplex and so, skin biopsy was done to confirm the diagnosis. On confirmation, patient’s parents were counselled about the disease and its management. <strong></strong></p>

scholarly journals Linear Psoriasis- A rare case report

2016 ◽  
Vol 8 (1) ◽  
pp. 74
Author(s):  
Md. Mahabubur Rahaman ◽  
Md Rahmat Ullah Siddique ◽  
Md Aminul Islam ◽  
Md. Moksedur Rahman ◽  
Md. Zahed Parvez Barbhuiyan ◽  
...  
Keyword(s):  
Case Report ◽  
Physical Examination ◽  
Skin Biopsy ◽  
Rare Case ◽  
Clinical History ◽  
Rare Form ◽  
Epidermal Nevus ◽  
Linear Pattern ◽  
Rare Case Report ◽  
Linear Psoriasis

Linear psoriasis is a rare form of disease which is very difficult to differentiate from inflammatory linear verrucous epidermal nevus. Sometimes clinical history, physical examination and histopathology analysis may not be sufficient to confirm the diagnosis. We report a case of25 year-old male presented with a linear plaque covered with silvery scales on left upper extremity extending from tip of the index to mid forearm for last 2 years. A skin biopsy was consistent with psoriasis, and the unilateral distribution in a linear pattern led to a diagnosis of linear psoriasis, which is a rare variant of psoriasis. Although histopathologically it can be difficult to distinguish from inflammatory linear verrucous epidermal nevus (ILVEN), linear psoriasis presents in adulthood and responds to conventional topical antipsoriatic therapies.

scholarly journals Dysgenetic Polycystic Disease of Minor Salivary Gland: A Rare Case Report and Review of the Literature

2017 ◽  
Vol 2017 ◽  
pp. 1-5
Author(s):  
N. Srikant ◽  
Shweta Yellapurkar ◽  
Karen Boaz ◽  
Mohan Baliga ◽  
Nidhi Manaktala ◽  
...  
Keyword(s):  
Differential Diagnosis ◽  
Salivary Gland ◽  
Case Report ◽  
Rare Case ◽  
Minor Salivary Gland ◽  
Rare Entity ◽  
Review Of The Literature ◽  
Lower Lip ◽  
Polycystic Disease ◽  
Rare Case Report

Polycystic (dysgenetic) disease of the salivary glands is a rare entity that has only recently been described in the literature. The disease is more commonly seen in females and majority of the cases have presented as bilateral parotid gland swellings. This case presenting in a 21-year-old male is the first of this unusual entity involving solely the minor salivary gland on the lower lip. This case report highlights the importance for the clinician to be aware of this differential diagnosis, when treating an innocuous lesion like a mucocele.

Necrotizing sialometaplasia of lower LIP-A rare case report

2017 ◽  
Vol 8 (1) ◽  
pp. 33
Author(s):  
Sonam Kohli ◽  
M.K. Sunil ◽  
Raghav Kumar ◽  
Aarti Trakroo ◽  
Saloni Arora
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Lower Lip ◽  
Rare Case Report ◽  
Necrotizing Sialometaplasia

scholarly journals A Rare Case Report of GVHD-related Cutaneous Horns of the lower lip.

2022 ◽  
Author(s):  
M. Verquin ◽  
C. Politis ◽  
F. Thonnart ◽  
S. Fransis ◽  
S. Schepers
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Lower Lip ◽  
Rare Case Report

Maffucci syndrome with the spindle cell hemangiomas in the mucosa of the lower lip: a rare case report and literature review

2013 ◽  
Vol 40 (7) ◽  
pp. 661-666 ◽  
Author(s):  
Yu Cai ◽  
Rong Wang ◽  
Xin-Ming Chen ◽  
Yi-Fang Zhao ◽  
Zhi-Jun Sun ◽  
...  
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Rare Case ◽  
Spindle Cell ◽  
Lower Lip ◽  
Maffucci Syndrome ◽  
Rare Case Report

scholarly journals Eugenol Hypersensitivity in Pediatric Dental Patient: A Rare Case Report

2016 ◽  
Vol 1 (2) ◽  
pp. 68-70
Author(s):  
Anant Gopal Nigam ◽  
Ankita Beniwal ◽  
Shefali Chaturvedi ◽  
Tanmay Bhatt
Keyword(s):  
Case Report ◽  
Hypersensitivity Reaction ◽  
Rare Case ◽  
Primary Teeth ◽  
Type I ◽  
Filling Material ◽  
Immediate Hypersensitivity ◽  
Lower Lip ◽  
Dental Patient ◽  
Rare Case Report

ABSTRACT Eugenol is a phenolic compound commonly used in dentistry as an analgesic and anti-inflammatory drug. Zinc oxide eugenol is an important root canal filling material in primary teeth with excellent documented success. Its cytotoxic effect is documented in some cases due to production of zinc eugenolate which is highly unstable and induces type IV hypersensitivity reactions and even generalized anaphylactic symptoms. But, the case reports documenting immediate hypersensitivity reaction to eugenol are very rare. This was a case of type I immediate hypersensitivity reaction to eugenol in a 3 years old pediatric patient. During the full mouth rehabilitation under general anesthesia, hard indurated swelling of lower lip was observed at the time of obturation of mandibular primary teeth. The procedure was stopped immediately suspecting an allergic response which was later confirmed to be eugenol allergy by patch test. Hence, it is important to evaluate all local allergies even if the patient fails to report allergy history. How to cite this article Beniwal A, Chaturvedi S, Bhatt T, Sharma A, Nigam AG. Eugenol Hypersensitivity in Pediatric Dental Patient: A Rare Case Report. J Mahatma Gandhi Univ Med Sci Tech 2016;1(2):68-70.

Hereditary Dystrophic Epidermolysis Bullosa A Rare Case Report

2015 ◽  
Vol 7 (2) ◽  
pp. 84-86
Author(s):  
Pallavi Urs ◽  
Shagun Sinha
Keyword(s):  
Case Report ◽  
Soft Tissue ◽  
Epidermolysis Bullosa ◽  
Rare Case ◽  
Diverse Group ◽  
Dystrophic Epidermolysis Bullosa ◽  
Tissue Separation ◽  
Rare Case Report ◽  
Oral Tissue ◽  
Care Practices

Abstract Epidermolysis bullosa (EB) is a diverse group of disorders characterized by blister formation with tissue separation occurring at variable depths in the skin and oral mucosa depending on the specific EB type. Oral tissue fragility and blistering is common to all EB types. However oral debilitation as a result of soft tissue scarring is primarily limited to the recessive dystrophic EB subtypes. Due to extreme mucosal fragility such patients are managed by modified dental care practices. This case report describes a rare case of recessive dystrophic EB. How to cite this article: Neena IE, Sinha S, Poornima P, Pallavi Urs. Hereditary Dystrophic Epidermolysis bullosa- A Rare Case Report. CODS J Dent 2015;7: 84-86

scholarly journals Lower Lip Sinus: A Rare Case Report

2016 ◽  
Vol 6 (10) ◽  
Author(s):  
Samoon Nuzhat ◽  
Hafiz Ather
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Lower Lip ◽  
Rare Case Report
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