scholarly journals Accelerated Phase of Chediak-Higashi Syndrome at Initial Presentation: A Case Report of an Uncommon Occurrence in a Rare Disorder

2015 ◽  
Author(s):  
Pooja Jaiswal
Keyword(s):  
Case Report ◽  
Initial Presentation ◽  
Rare Disorder ◽  
Chediak Higashi Syndrome

Acute pulmonary edema as the initial presentation of a pheochromocytoma: case report

2013 ◽  
Author(s):  
Eduarda Resende ◽  
Maritza Sa ◽  
Margarida Ferreira ◽  
Silvestre Abreu
Keyword(s):  
Case Report ◽  
Pulmonary Edema ◽  
Initial Presentation ◽  
Acute Pulmonary Edema

scholarly journals Adrenergic cardiomyopathy and cardiogenic shock as initial presentation of pheochromocytoma. A case report and review of the literature

2018 ◽  
Vol 49 ◽  
pp. 145-148 ◽  
Author(s):  
Esther Gil-Barrionuevo ◽  
José Maria Balibrea ◽  
Enric Caubet ◽  
Oscar Gonzalez ◽  
Ramón Vilallonga ◽  
...  
Keyword(s):  
Case Report ◽  
Cardiogenic Shock ◽  
Initial Presentation ◽  
Review Of The Literature

Placental mesenchymal dysplasia- A case report

2021 ◽  
Vol 6 (3) ◽  
pp. 249-252
Author(s):  
Zeba Nisar ◽  
Mahendra A Patil ◽  
Vaishali J Pol ◽  
Jaydeep N Pol
Keyword(s):  
Case Report ◽  
Histopathological Examination ◽  
Clinical Suspicion ◽  
Termination Of Pregnancy ◽  
Rare Disorder ◽  
Molar Pregnancy ◽  
Female Fetus ◽  
Beta Hcg ◽  
Antenatal Visits ◽  
Placental Mesenchymal Dysplasia

Placental mesenchymal dysplasia is a rare disorder mainly characterized by enlarged placenta. Patients on antenatal visits present with normal or slightly raised Beta-HCG, raised Alfa-fetoprotein and cystic structures on USG resembling a molar pregnancy. It has to be differentiated from molar pregnancies to avoid unnecessary termination of pregnancy. This condition is associated with IUGR or IUFD. Mostly the fetus are females. Due to lack of awareness of this condition it remains underreported. Here we present a case report of 20 years old female 37 week pregnant with IUGR with clinical suspicion of molar pregnancy gave birth to alive female fetus and on histopathological examination of placenta was diagnosed with PMD.

Intermediate cell histiocytosis: a case report of a rare disorder

2004 ◽  
Vol 50 (3) ◽  
pp. P115
Author(s):  
Ayad E. Abrou ◽  
Ethan Nydorf ◽  
Christine Adamick
Keyword(s):  
Case Report ◽  
Rare Disorder ◽  
Intermediate Cell

scholarly journals Graham-Little Piccardi Lassueur Syndrome: case report

2012 ◽  
Vol 87 (5) ◽  
pp. 775-777 ◽  
Author(s):  
Raquel Bissacotti Steglich ◽  
Renata Elise Tonoli ◽  
Giselle Martins Pinto ◽  
Fernanda Melo Müller ◽  
Isabelle Maffei Guarenti ◽  
...  
Keyword(s):  
Case Report ◽  
Physical Examination ◽  
Hair Follicles ◽  
Rare Disorder ◽  
Rare Syndrome ◽  
Scarring Alopecia ◽  
History Of

A 33-year-old woman presented with a 3-year history of progressive alopecia of the scalp. Past treatment with hydroxicloroquine did not show improvement. Physical examination revealed multiple areas of alopecia with atrophic aspect of the scalp, and axillary and pubic hypotrichosis. Dermoscopy showed hyperkeratosis and accentuation of follicular ostia. Anatomopathological examination revealed decrease in the number of hair follicles, upper perifollicular infiltrate and areas with fibrosis. The Piccardi-Lassueur-Graham-Little syndrome is a rare disorder, characterized by the triad of multifocal scarring alopecia of the scalp, keratotic follicular eruption and hypotrichosis of axillary and pubic regions. Management is a challenge and many medications tried have controversial results. We report a case of this rare syndrome which improved with corticoids.

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