scholarly journals Sweet's syndrome leading to acquired cutis laxa in a child (Marshall's syndrome): A rare case report

2016 ◽  
Vol 17 (2) ◽  
pp. 135
Author(s):  
H Bangaru ◽  
KAK Surendran ◽  
BL Nanjundaswamy ◽  
B Vijaya
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Cutis Laxa ◽  
Sweet’S Syndrome ◽  
Sweet's Syndrome ◽  
Rare Case Report

scholarly journals Pulmonary and Central Nervous System Involvement in Sweet's Syndrome: A Very Rare Case Report

2008 ◽  
Vol 47 (16) ◽  
pp. 1481-1484 ◽  
Author(s):  
Hande Aydemir ◽  
Nefise Öztoprak ◽  
Güven Celebi ◽  
Cevdet Altinyazar ◽  
Figen Barut ◽  
...  
Keyword(s):  
Central Nervous System ◽  
Nervous System ◽  
Case Report ◽  
Rare Case ◽  
Central Nervous System Involvement ◽  
Sweet’S Syndrome ◽  
Sweet's Syndrome ◽  
System Involvement ◽  
Rare Case Report

scholarly journals Bullous Sweet’s syndrome in a patient with ulcerative colitis: a rare case report

2020 ◽  
Vol 29 (3) ◽  
Author(s):  
Melania Giannoni ◽  
Giulio Rizzetto ◽  
Claudia Sapigni ◽  
Matteo Paolinelli ◽  
Corrado Tagliati ◽  
...  
Keyword(s):  
Ulcerative Colitis ◽  
Case Report ◽  
Rare Case ◽  
Sweet’S Syndrome ◽  
Sweet's Syndrome ◽  
Rare Case Report

Acquired cutis laxa secondary to Sweet syndrome in a child (Marshall syndrome): A rare case report

2019 ◽  
Vol 47 (2) ◽  
pp. 146-149
Author(s):  
Ashish Jagati ◽  
Shivank Shrivastava ◽  
Bhavna Baghela ◽  
Pooja Agarwal ◽  
Siddhartha Saikia
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Cutis Laxa ◽  
Sweet Syndrome ◽  
Rare Case Report

scholarly journals A rare case of subcutaneous Sweet’s syndrome in a patient with chronic myelogenous leukemia: a case report and review of the literature

2014 ◽  
Vol 7 (2) ◽  
pp. 79-83
Author(s):  
Congli Wang ◽  
Mary Ellen Martin ◽  
Roberta E. Smith ◽  
Deline DaCosta ◽  
Raghava Levaka Veera ◽  
...  
Keyword(s):  
Case Report ◽  
Chronic Myelogenous Leukemia ◽  
Rare Case ◽  
Myelogenous Leukemia ◽  
Sweet’S Syndrome ◽  
Review Of The Literature ◽  
Sweet's Syndrome

A rare case report of elastosis perforans serpiginosa in acquired cutis laxa

2021 ◽  
Vol 7 (3) ◽  
pp. 268-271
Author(s):  
R Roja ◽  
Ramanamurthy Pemmaraju ◽  
Krishnarao V Pasagadugula ◽  
Raajitha N S S Penugonda
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Neck Region ◽  
Cutis Laxa ◽  
Histopathological Features ◽  
Central Depression ◽  
Rare Case Report

Elastosis perforans serpiginous (EPS) is a rare perforating disorder characterized by trans epidermal elimination of fragmented elastic fibres.The cutaneous features include asymptomatic hyperkeratotic papules. Here we present a case of 27-year old female presented with hyperkeratotic papules with central depression arranged transversely in a serpiginous fashion on front of the laxed skin of the neck region. The histopathological features are consistent with the features of EPS on Cutis Laxa. Elastosis perforans serpiginosa in Acquired cutis laxa has not been reported very rarely, hence this case has been reported.

Primary neuroendocrine carcinoma of renal: a rare case report

2014 ◽  
Author(s):  
Tadeusz Budlewski ◽  
Dorota Szydlarska ◽  
Norbert Szalus ◽  
Jolanta Kijek ◽  
Beata Ewa Chrapko
Keyword(s):  
Case Report ◽  
Neuroendocrine Carcinoma ◽  
Rare Case ◽  
Rare Case Report

Combination of turner syndrome and congenital adrenal hyperplasia: a rare case report

2017 ◽  
Author(s):  
Ivana Sagova ◽  
Dušan Pavai ◽  
Matej Stančik ◽  
Helena Urbankova ◽  
Juliana Gregova ◽  
...  
Keyword(s):  
Case Report ◽  
Congenital Adrenal Hyperplasia ◽  
Turner Syndrome ◽  
Rare Case ◽  
Adrenal Hyperplasia ◽  
Rare Case Report
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