Premature Infant with Haemophilus parainfluenzae Sepsis: Case Report and Literature Review

2019 ◽  
Vol 65 (6) ◽  
pp. 638-641
Author(s):  
Mohammed A Alsuhaibani
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Premature Infant ◽  
Rare Case ◽  
Causative Organism ◽  
Mortality And Morbidity ◽  
Haemophilus Parainfluenzae ◽  
Early Onset Sepsis ◽  
Invasive Bacterial Infection ◽  
Adults And Children

Abstract Haemophilus parainfluenzae is an unusual causative organism of invasive bacterial infection in adults and children. Mortality and morbidity secondary to Haemophilus parainfluenzae have been documented in the literature. We present a rare case of a premature infant with early onset sepsis caused by Haemophilus parainfluenzae, who was born to a primigravida with chorioamnionitis. The infant was successfully treated for 10 days with antibiotics with no complications.

Hydrops fetalis And Congenital Pulmonary Capillary Haemangiomatosis in a Premature Infant, A Case Report And Literature Review

2018 ◽  
Author(s):  
A Iacoi ◽  
A Brobeil ◽  
M Goette ◽  
C Enzensberger ◽  
V Mueller ◽  
...  
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Premature Infant ◽  
Hydrops Fetalis ◽  
Pulmonary Capillary

Popliteal nodal metastasis from squamous cell cancer of the foot. Case report and literature review

2019 ◽  
pp. 1-2
Keyword(s):  
Case Report ◽  
Lymph Node ◽  
Literature Review ◽  
Squamous Cell ◽  
Rare Case ◽  
Squamous Cell Cancer ◽  
Cell Cancer ◽  
Nodal Metastasis ◽  
Regional Disease ◽  
The Right

We report a very rare case of squamous cell cancer of the right foot which had metastasize to the ipsilateral popliteal lymph node after initial diagnosis and treatment for the loco-regional disease.

A rare case of heterotopic pregnancy after a single embryo transfer: A case report and literature review

2021 ◽  
Author(s):  
Satoshi Hosoya ◽  
Yuta Kasahara ◽  
Hiromi Komazaki ◽  
Hiroshi Kishi ◽  
Hirokuni Takano ◽  
...  
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Embryo Transfer ◽  
Rare Case ◽  
Single Embryo Transfer ◽  
Heterotopic Pregnancy

scholarly journals Bilateral Florid Papillomatosis of the Nipple: An Unusual Indicator for Metachronous Breast Cancer Development—A Case Report

2014 ◽  
Vol 2014 ◽  
pp. 1-3 ◽  
Author(s):  
Walid Sasi ◽  
Dibyesh Banerjee ◽  
Kefah Mokbel ◽  
Anup K. Sharma
Keyword(s):  
Breast Cancer ◽  
Case Report ◽  
Literature Review ◽  
Papillary Carcinoma ◽  
Rare Case ◽  
Benign Disease ◽  
Cancer Development ◽  
Breast Cancer Development ◽  
Histopathological Features ◽  
Metachronous Breast Cancer

Adenoma or florid papillomatosis of the nipple (FPN) is a rare benign disease which has histopathological features similar to those of a mammary papillary carcinoma. Here, we report a rare case of bilateral florid papillomatosis of the nipple and breast cancer, with a literature review.

scholarly journals An unusual Wilms tumor with urethral recurrence: rare case report and literature review

2015 ◽  
Vol 2 (4) ◽  
Author(s):  
Elizaveta Chernetsova ◽  
Ahmed Nasr ◽  
Luis Gerra ◽  
Bilaal Kabir ◽  
Marie JeongMin Kim ◽  
...  
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Rare Case ◽  
Wilms Tumor ◽  
Rare Case Report ◽  
Urethral Recurrence

scholarly journals Non-painful severe variant form of eruptive lingual papillitis: A case report and literature review

2021 ◽  
Vol 13 (2) ◽  
Author(s):  
Manal Ahmed Halwani
Keyword(s):  
Emergency Department ◽  
Case Report ◽  
Literature Review ◽  
Oral Hygiene ◽  
Rare Case ◽  
Dorsal Surface ◽  
Variant Form ◽  
Girl Child ◽  
Rare Case Report ◽  
History Of

Eruptive lingual papillitis is a common benign disorder manifested by inflammation of fungiform papillae on the dorsolateral surface of the tongue. Several variants of lingual papillitis have been reported since 1997, most or all of them with painful erythematous papules. Here we report a case of 6 years old girl child with non-painful severe variant form of eruptive lingual papillitis presented to the emergency department. The entire dorsal surface of the tongue was surfaced by 2-3mm by multiple erythematous papules and some with a white or yellowish colour. The papules were excessively inflamed, pigmented, aggregated, and crusted. The cause was idiopathic which resolved within ten days. The parent and patient were reassured with advice to practice oral hygiene. This is a rare case report describing non-painful lingual papillitis without a history of any prior episodes.

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