scholarly journals A case report of dyshidrotic bullous pemphigoid developing after partial anterior circulation ischaemic stroke

2021 ◽  
Vol 2021 (3) ◽  
Author(s):  
D Fanelli ◽  
J Miller ◽  
R Setty ◽  
E Husain ◽  
M McNeil
Keyword(s):  
Case Report ◽  
Ischaemic Stroke ◽  
Bullous Pemphigoid ◽  
Cerebrovascular Disorders ◽  
Skin Condition ◽  
Interesting Case ◽  
Rare Form ◽  
Anterior Circulation ◽  
Hands And Feet

ABSTRACT Dyshidrotic bullous pemphigoid is a rare form of bullous pemphigoid that affects predominantly a patient’s hands and feet. It has been associated in the literature with neurologic, psychiatric and cerebrovascular disorders. We present an interesting case of this rare skin condition developing in a patient following a diagnosis of partial anterior circulation stroke.

scholarly journals Cutaneous Polyarteritis Nodosa (cPAN) in ab 5 Years Old Girl

2018 ◽  
Vol 2 (5) ◽  
Author(s):  
Lubna Nazir
Keyword(s):  
Case Report ◽  
Skin Biopsy ◽  
Polyarteritis Nodosa ◽  
Clinical Course ◽  
Systemic Vasculitis ◽  
Separate Entity ◽  
Rare Form ◽  
Cutaneous Polyarteritis Nodosa ◽  
True Incidence ◽  
Hands And Feet

Polyarteritis nodosa is a rare form of systemic vasculitis. Cutaneous polyarteritis nodosa (cPAN) is subtype of systemic PAN which predominantly affects the skin, extra-cutaneous findings include fever, malaise, myalgias, arthralgias, and neuropathy. The true incidence of cutaneous PAN is unknown. cPAN is recognized as a separate entity and is essentially a benign disorder which should be distinguished from systemic PAN, as the clinical course and management of the two conditions is different. In this case report, we have described a patient with fever and gangrene of both hands and feet. The patient underwent a very extensive workup in order to determine the cause of her condition, which finally turned out cPAN on skin biopsy

scholarly journals Acral pityriasis rosea: A rare variant of pityriasis rosea

2021 ◽  
Vol 13 (1) ◽  
Author(s):  
Pimpa Tantanasrigul ◽  
Mingkwan Wichaidit ◽  
Preya Kullavanijaya
Keyword(s):  
Rare Variant ◽  
Skin Condition ◽  
Rare Form ◽  
Pityriasis Rosea ◽  
Atypical Manifestations ◽  
Inflammatory Skin ◽  
The Difference ◽  
Hands And Feet

Pityriasis rosea (PR) is a common, selflimited inflammatory skin condition, usually affects the trunk and proximal extremities. A variety of atypical manifestations of PR have been recognized ranging from the difference in the morphology, distribution, and course. Herein, the rare form of acral PR in an adult has been illustrated as the 29- year-old Thai female who presented with generalized erythematous papules and plaques with peripheral collarette scales on the trunk and extremities, prominently on the hands and feet.[...]

Bullous Pemphigoid in Infancy: A Case Report

PEDIATRICS ◽  
1977 ◽  
Vol 59 (6) ◽  
pp. 942-945
Author(s):  
William M. Gould ◽  
David A. Zlotnick
Keyword(s):  
Case Report ◽  
Bullous Pemphigoid ◽  
Oral Lesions ◽  
Bullous Eruption ◽  
Hands And Feet

Bullous pemphigoid occurs rarely in children. Bean and Jordan1 found only eight cases reported as of 1974 and the youngest of these patients was 2 years of age. Presented here is the case of a 3½-month-old infant who developed this disease. CASE REPORT A 3½-month-old boy developed a progressively spreading bullous eruption (Fig. 1 and 2). Within a week the hands and feet were covered with large, tense bullae lying on a base of erythema, and scattered vesicles appeared on the back of the neck, the trunk, and the rims of the ears. There were no oral lesions. The child was fussy and irritable but had no fever.

Abstract #230: Bullous Pemphigoid-Adverse Reaction to Linagliptin (Tradjenta): A Case Report

2015 ◽  
Vol 21 ◽  
pp. 38-39
Author(s):  
Issac Sachmechi ◽  
Raya Galibov ◽  
Venkat Dirish Arukala
Keyword(s):  
Adverse Reaction ◽  
Case Report ◽  
Bullous Pemphigoid

Cystic struma ovarii, a rare form of ovarian tumor – a case report, and review of the literature

2007 ◽  
Vol 148 (48) ◽  
pp. 2285-2287 ◽  
Author(s):  
Gabriella Östör ◽  
Ildikó Tóth ◽  
Zsuzsanna Hrubyné Tóth ◽  
Sándor Bazsa
Keyword(s):  
Case Report ◽  
Ovarian Tumor ◽  
Ca 125 ◽  
Struma Ovarii ◽  
Review Of The Literature ◽  
Rare Form

Az ovarialis strumák a petefészek-teratomák kevesebb mint 3%-át adják. Megjelenhet bennük a pajzsmirigy szinte minden betegsége, és előfordulhat malignitás is. A szerzők esetében egy 31 éves nő bal oldali petefészekcisztáját távolították el, amely az ovariumcarcinoma klinikai tüneteit mutatta, úgymint nagy hasi térfoglalás, ascites, emelkedett szérum-CA 125-szint. A szövettani diagnózis benignus struma ovarii volt. A posztoperatív pajzsmirigyműködés normális maradt.

Psoriasis vulgaris accompanied by bullous pemphigoid: A case report.

1988 ◽  
Vol 50 (6) ◽  
pp. 1018-1021 ◽  
Author(s):  
Nobuaki TAKE ◽  
Tetsuya HIRANO ◽  
Osamu IYOTA ◽  
Yoshinori SUENAGA
Keyword(s):  
Case Report ◽  
Bullous Pemphigoid ◽  
Psoriasis Vulgaris

scholarly journals Surgical Thrombectomy After Large Vessel Ischaemic Stroke: A Case Report

2021 ◽  
Vol 50 ◽  
pp. 46-47
Author(s):  
João S. Peixoto ◽  
José P. Brandão ◽  
Clara Nogueira ◽  
Andreia Coelho ◽  
Rita Augusto ◽  
...  
Keyword(s):  
Case Report ◽  
Ischaemic Stroke ◽  
Large Vessel ◽  
Surgical Thrombectomy

scholarly journals A Case Report of Semaglutide-associated Bullous Pemphigoid

2021 ◽  
Author(s):  
Clayton P. Burruss ◽  
Jordan M. Jones ◽  
Jyoti B. Burruss
Keyword(s):  
Case Report ◽  
Bullous Pemphigoid

scholarly journals Case Report: Rivaroxaban-associated Bullous Pemphigoid in A Patient with Atrial Fibrillation

CJC Open ◽  
2021 ◽  
Author(s):  
Jiaming (Calvin) Liang ◽  
Karanvir Raman ◽  
Siu Him Chan ◽  
A. Yashar Tashakkor
Keyword(s):  
Atrial Fibrillation ◽  
Case Report ◽  
Bullous Pemphigoid

Sonographic Diagnosis of Bilateral Tubal Pregnancies

2021 ◽  
pp. 875647932199235
Author(s):  
Amber R. Matuzak
Keyword(s):  
Case Report ◽  
Early Diagnosis ◽  
Tubal Ligation ◽  
Tubal Pregnancy ◽  
Rare Form ◽  
Sonographic Diagnosis ◽  
Ectopic Pregnancies ◽  
The Right ◽  
Preoperative Sonography ◽  
Bilateral Tubal Pregnancy

Bilateral tubal pregnancy (BTP) is a very rare form of ectopic twin gestation. Many times, they occur after the use of assisted reproductive therapy. Most cases of BTP are diagnosed during laparoscopy. This case report demonstrates a rare preoperative, sonography diagnosis of a spontaneous BTP which occurred after a tubal ligation. The sonogram revealed two corpus luteal cysts, both located on the right ovary, which suggests that the left tubal pregnancy most likely occurred as a result of ovum transmigration. This case demonstrates the important role that sonography plays in the early diagnosis of ectopic pregnancies as well as the importance of thoroughly examining the entire pelvis during a pelvic sonogram.

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