Scrofuloderma "bridges" as a rare form of late syphilis

1930 ◽  
Vol 26 (9) ◽  
pp. 943-943
Author(s):  
A. Dmitriev
Keyword(s):  
Specific Treatment ◽  
Rare Form ◽  
Typical Picture ◽  
Late Syphilis

Abstracts. Venereology and Dermatology. Scrofuloderma "bridges" as a rare form of late syphilis .. Schmidt. (Derm. Ztsch. Bd. 57, H. 5) describes a case clinically similar to scrofuloderma, where the picture showed the presence of typical "bridges" - scars. so common in scrophuloderma. However, the study of these scars by sections gave a typical picture for a syphilitic process. The specific treatment of this case was soon brilliant.

scholarly journals Myositis gummosa

2021 ◽  
Vol 25 (11) ◽  
pp. 1237-1237
Author(s):  
A. Dmitriev
Keyword(s):  
Specific Treatment ◽  
Late Syphilis ◽  
Different Parts

A. Jordan and Popova-Bloom (Derm. Zisch., Bd. 55, H. 2) as a result of their observations of 8 cases of this disease come to the following conclusions that m. g. can occur in different parts of the muscles, but more often affect m. sternocleidomastoideus, women are more likely to suffer (the authors have one man out of 8 cases), because this disease is observed in individuals with lues ignorata. M. g. is a manifestation of late syphilis. Diagnosis is fraught with great difficulties and is facilitated only by a positive R. W. The prognosis is favorable, for specific treatment quickly leads to a cure.

“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

A multicentre randomized controlled trial on trans-generational attention deficit/hyperactivity disorder (ADHD) in mothers and children (AIMAC): an exploratory analysis of predictors and moderators of treatment outcome

2019 ◽  
Vol 47 (1) ◽  
pp. 49-65 ◽  
Author(s):  
Charlotte Jaite ◽  
Betteke Maria van Noort ◽  
Timo D. Vloet ◽  
Erika Graf ◽  
Viola Kappel ◽  
...  
Keyword(s):  
Treatment Outcome ◽  
Primary Outcome ◽  
Controlled Trial ◽  
Specific Treatment ◽  
Externalizing Symptoms ◽  
Control Treatment ◽  
Comorbid Depression ◽  
Adhd Treatment ◽  
Mothers And Children ◽  
Maternal Adhd

Abstract. Objective: We examined predictors and moderators of treatment outcome in mothers and children diagnosed with ADHD in a large multicentre RCT. Method: In total, 144 mother-child dyads with ADHD were randomly assigned to either a maternal ADHD treatment (group psychotherapy and open methylphenidate medication, TG) or to a control treatment (individual counselling without psycho- or pharmacotherapy, CG). After maternal ADHD treatment, parent-child training (PCT) for all mother-child dyads was added. The final analysis set was based on 123 dyads with completed primary outcome assessments (TG: n = 67, CG: n = 56). The primary outcome was the change in each child’s externalizing symptoms. Multiple linear regression analyses were performed. Results: The severity of the child’s externalizing problem behaviour in the family at baseline predicted more externalizing symptoms in the child after PCT, independent of maternal treatment. When mothers had a comorbid depression, TG children showed more externalizing symptoms after PCT than CG children of depressive mothers. No differences between the treatment arms were seen in the mothers without comorbid depression. Conclusions: Severely impaired mothers with ADHD and depressive disorder are likely to need additional disorder-specific treatment for their comorbid psychiatric disorders to effectively transfer the contents of the PCT to the home situation (CCTISRCTN73911400).

The Male Batterer: Still Waiting for Specific Treatment

1986 ◽  
Vol 31 (11) ◽  
pp. 897-898
Author(s):  
Louis B. Schlesinger
Keyword(s):  
Specific Treatment ◽  
Male Batterer

Conjoint or Gender-Specific Treatment for Partner Abuse?

2000 ◽  
Author(s):  
K. D. O'Leary ◽  
R. E. Heyman ◽  
P. H. Neidig
Keyword(s):  
Partner Abuse ◽  
Specific Treatment ◽  
Gender Specific

The Natural Course of Defibrination Syndrome Caused by Echis Colorata Venom in Man

1974 ◽  
Vol 31 (03) ◽  
pp. 420-428 ◽  
Author(s):  
M Fainaru ◽  
S Eisenberg ◽  
N Manny ◽  
C Hershko
Keyword(s):  
Factor Viii ◽  
Blood Coagulation ◽  
Major Bleeding ◽  
Renal Damage ◽  
Specific Treatment ◽  
Natural Course ◽  
Factor V ◽  
Thrombocyte Count

SummaryThe natural course of defibrination syndrome caused by Echis colorata venom (ECV) in five patients is reported. All patients developed afibrinogenemia within six hours after the bite. Concomitantly a depression in factor V was recorded. Factor VIII and thrombocyte count in blood were normal in most patients. In the light of the known effects of ECV on blood coagulation in vivo and in vitro it is concluded that the afibrinogenemia is due to intravascular clotting.Four patients had transient renal damage, manifested by oliguria, azotemia, albuminuria and cylindruria, ascribed to microthrombi in the renal glomeruli.After the bite, the natural course was benign, no major bleeding was observed, and all signs of coagulopathy reverted to normal within 7 days. Therefore we recommend no specific treatment for this condition. In the case of heavily bleeding patients, administration of antiserum against ECV and/or heparin should be considered.

Hypercoagulability and High Lipoprotein(a) Levels in Patients with Central Retinal Vein Occlusion

1994 ◽  
Vol 72 (01) ◽  
pp. 039-043 ◽  
Author(s):  
Francesco Bandello ◽  
Silvana Vigano’ D’Angelo ◽  
Mariella Parlavecchia ◽  
Alessandra Tavola ◽  
Patrizia Della Valle ◽  
...  
Keyword(s):  
Retinal Vein Occlusion ◽  
Central Retinal Vein Occlusion ◽  
Specific Treatment ◽  
Fibrin Deposition ◽  
Heparin Cofactor Ii ◽  
Lipoprotein A ◽  
Vein Occlusion ◽  
Acute Event ◽  
D Dimer ◽  
Central Retinal Vein

SummaryA series of coagulation parameters and lipoprotein(a) (Lp(a)) were explored in plasma from 40 patients with central retinal vein occlusion (CRVO, non-ischemic type n = 12; ischemic type n = 28) free of local and systemic predisposing factors, 1 to 12 months after the acute event. Forty age- and sex-matched patients with cataract served as controls. Prothrombin fragment 1.2 (FI.2), D-dimer, FVII:C - but not FVII: Ag - were higher and fibrinogen was lower in CRVO patients than in controls. Patients with non-ischemic CRVO had higher FI .2 and FVII:C and lower heparin cofactor II than patients with ischemic CRVO. Lp(a) levels greater than 300 mg/1 were observed in 12 patients with CRVO and in 4 controls (30% vs 10%, p <0.025). Patients with high Lp(a) - consistently associated with the S2 phenotype - had higher FVII:C, FVII:C/Ag ratio, and fibrinogen than the remaining CRVO patients. Plasma FI.2 and D-dimer correlated fairly in controls (r = 0.41) and patients with normal Lp(a) levels (r = 0.55), but they did not in the group of patients with high Lp(a) (r = 0.19), where the latter parameter was negatively related to D-dimer (r = −0.55). There was no dependence of the abnormalities observed on the time elapsed from vein occlusion. The findings of activated FVII and high FI.2, D-dimer, and Lp(a) are not uncommon in patients with CRVO. Increased thrombin formation with fibrin deposition and impaired fibrinolysis may play a role in the pathophysiology of CRVO and require specific treatment

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.

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