Morphological Observations of a Rare Form of Spiniferomonas, S. cf. annulata (Chrysophyceae: Paraphysomonadaceae)

1994 ◽  
Vol 113 (3) ◽  
pp. 406 ◽  
Author(s):  
Daniel E. Wujek ◽  
Charles J. O'Kelly ◽  
L. C. Saha
Keyword(s):  
Rare Form

“Upside Down Stomach”: Rare Form of Diaphragmatic Hernia

1952 ◽  
Vol 21 (2) ◽  
pp. 300-303 ◽  
Author(s):  
Raymond A. Gagliardi
Keyword(s):  
Diaphragmatic Hernia ◽  
Rare Form

DYT11- Myoclonic Dystonia as a rare form of childhood dystonia

2006 ◽  
Vol 37 (06) ◽  
Author(s):  
S von Spiczak ◽  
B Petersen ◽  
H Muhle ◽  
C Klein ◽  
U Stephani
Keyword(s):  
Rare Form

Morgagni hernia – case reports

2020 ◽  
Vol 99 (7) ◽  
Keyword(s):  
Diaphragmatic Hernia ◽  
Case Reports ◽  
Congenital Defect ◽  
Morgagni Hernia ◽  
Rare Form

Morgagni hernia is a rare form of diaphragmatic hernia. It is a congenital defect of the diaphragm, often asymptomatic in adulthood and thus usually found only incidentally. Its treatment is predominantly surgical. This article presents three case reports of patients operated in our department.

Diagnosis and Ablation of Fascicular Tachycardia

2011 ◽  
Vol 3 (1) ◽  
pp. 67
Author(s):  
Akihiko Nogami ◽  
Keyword(s):  
Ventricular Tachycardia ◽  
Right Bundle Branch Block ◽  
Axis Deviation ◽  
Exit Site ◽  
Rare Form ◽  
Bundle Branch Block ◽  
Diagnosis And Therapy ◽  
Narrow Qrs ◽  
Left Posterior ◽  
Qrs Morphology

Verapamil-sensitive fascicular ventricular tachycardia (VT) is the most common form of idiopathic left VT. According to the QRS morphology and the successful ablation site, left fascicular VT can be classified into three subgroups: left posterior fascicular VT, whose QRS morphology shows right bundle branch block (RBBB) configuration and superior axis (common form); left anterior fascicular VT, whose QRS morphology shows RBBB configuration and right-axis deviation (uncommon form), and upper septal fascicular VT, whose QRS morphology shows narrow QRS configuration and normal or right-axis deviation (rare form). Posterior and anterior fascicular VT can be successfully ablated at the posterior or anterior mid-septum with a diastolic Purkinje potential during VT or at the VT exit site with a fused pre-systolic Purkinje potential. Upper septal fascicular VT can also be ablated at the site with diastolic Purkinje potential at the upper septum. Recognition of the heterogeneity of this VT and its unique characteristics should facilitate appropriate diagnosis and therapy.

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.

Aspirine asthma in children - not a rare form of disease

2015 ◽  
Vol 72 (8) ◽  
pp. 99-106
Author(s):  
Е.N. Оkhotnikova ◽  
◽  
L.V. Duda ◽  
G.V. Shklyarska ◽  
◽  
...  
Keyword(s):  
Rare Form ◽  
Asthma In Children

Case of follow-up and successful surgical treatment rare form of subaortic membrane in infant

2017 ◽  
Vol 14 (3) ◽  
pp. 161-165
Author(s):  
A.I. Kim ◽  
Т.V. Rogova ◽  
R.М. Кurganov ◽  
Е.V. Kholmanskaya
Keyword(s):  
Surgical Treatment ◽  
Rare Form ◽  
Subaortic Membrane

A RARE FORM OF HYPOPHOSPHATEMIC RICKETS DUE TO MUTATIONS IN THE SLC34A3 GENE: DIAGNOSIS AND TREATMENT PECULIARITIES

2018 ◽  
Vol 97 (6) ◽  
pp. 69-73
Author(s):  
E.A. Nikolaeva ◽  
◽  
S.Yu. Kuznetsova ◽  
V.Yu. Voinova ◽  
Yu.I. Davydova ◽  
...  
Keyword(s):  
Diagnosis And Treatment ◽  
Hypophosphatemic Rickets ◽  
Rare Form ◽  
Gene Diagnosis

Prenatal diagnosis of rare form chromosomal pathology: double aneuploidy

2019 ◽  
Author(s):  
L.A. Khlevnaya, S.A. Malova, L.I. Mitusova
Keyword(s):  
Prenatal Diagnosis ◽  
Clinical Manifestation ◽  
Rare Form ◽  
Chromosomal Disease ◽  
Phenotypic Features ◽  
Double Aneuploidy

The article represents the double aneuploidy, a rare form of chromosome pathology. 6 cases of double aneuploidy were diagnosed prenatally and 1 case was diagnosed postnatal. A variety of ultrasound signs is shown in this chromosomal pathology. The prevalence of phenotypic features of the chromosomal disease, which has the greatest clinical manifestation, was noted.

scholarly journals Primary breast tuberculosis: imaging findings of a rare disease

2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Ali H. Baykan ◽  
Hakan S. Sayiner ◽  
Ibrahim Inan ◽  
Elcin Aydin ◽  
Sukru M. Erturk
Keyword(s):  
Differential Diagnosis ◽  
Rare Disease ◽  
Extrapulmonary Tuberculosis ◽  
Reproductive Age ◽  
Malignant Diseases ◽  
Imaging Findings ◽  
Granulomatous Mastitis ◽  
Rare Form ◽  
Breast Tuberculosis

AbstractBreast tuberculosis is a rare form of extrapulmonary tuberculosis which tends to affect females of reproductive age, and is much rarer in males, postmenopausal women, and pre-pubescent girls. It is difficult to diagnose because it can mimic benign conditions such as a fibroadenoma, as well as malignant diseases like a carcinoma. It is also particularly difficult to distinguish breast tuberculosis from granulomatous mastitis, so other possible diagnoses should be ruled out first. The diagnosis of breast tuberculosis has three essential pillars: clinical examination, radiological evaluations, and histopathological sampling. Radiological evaluations are not only critical in diagnosis but are also important in the planning of the treatment and during the follow-up. This paper aims to review the imaging findings and the differential diagnosis of breast tuberculosis.

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