Hemicrania Continua Responsive to Intravenous Methyl Prednisolone

2010 ◽  
Vol 2010 ◽  
pp. 68-69
Author(s):  
A. Panagariya
2009 ◽  
Vol 49 (4) ◽  
pp. 604-607 ◽  
Author(s):  
Sanjay Prakash ◽  
Krutik J. Brahmbhatt ◽  
Niraj T. Chawda ◽  
Nidhhi Tandon

Author(s):  
F. G. Zaki

Fetal and neonatal liver injury induced by agents circulating in maternal plasma, even though well recognized, its morphological manifestations are not yet established. As part of our studies of fetal and neonatal liver injury induced by maternal nutritional disorders, metabolic impairment and toxic agents, the effects of two anti-inflammatory steroids have been recently inves tigated.Triamcinolone and methyl prednisolone were injected each in a group of rats during pregnancy at a-dosage level of 2 mgm three times a week. Fetal liver was studied at 18 days of gestation. Litter size and weight markedly decreased than those of control rats. Stillbirths and resorption were of higher incidence in the triamcinolone group than in those given the prednisolone.


2007 ◽  
Vol 26 (03) ◽  
pp. 186-199 ◽  
Author(s):  
A. May ◽  
P. Kropp ◽  
Z. Katsarava ◽  
G. Haag ◽  
C. Lampl ◽  
...  

ZusammenfassungDie IHS-Kriterien definieren vier primäre Kopfschmerzerkrankungen, die zu täglichen Dauerkopfschmerzen führen können: 1) chronische Migräne, 2) Kopfschmerz vom Spannungstyp, 3) Hemicrania continua, 4) neu aufgetretener Kopfschmerz. In der Praxis ist davon häufig der Kopfschmerz durch Medikamentenübergebrauch (früher: Analgetikakopfschmerz) abzugrenzen. Die jetzt von der Deutschen, Österreichischen und Schweizer Kopfschmerzgesellschaft gemeinsam vorgelegte Therapieleitlinie fasst die Literatur zur Therapie dieser Kopfschmerzformen zusammen und gibt Therapieempfehlungen, die die Literaturevidenz, aber auch die Praktikabilität berücksichtigen.


2009 ◽  
Vol 28 (06) ◽  
pp. 356-360
Author(s):  
A. May ◽  
W. Paulus ◽  
T.-M. Wallasch ◽  
A. Straube

ZusammenfassungDie IHS-Kriterien definieren vier primäre Kopfschmerzerkrankungen, die zu täglichen Dauerkopfschmerzen führen können: chronische Migräne, Kopfschmerz vom Spannungstyp, Hemicrania continua und neu aufgetretener Kopfschmerz. Abzugrenzen ist der als ein sekundärer Kopfschmerz klassifizierte Kopfschmerz durch Medikamentenübergebrauch (früher: Analgetikakopfschmerz). Zu der häufigsten primären Form gehört die chronische Migräne, bei der in etwa 80% ein Medikamentenübergebrauch beobachtet werden kann. In diesem Rahmen wird diskutiert, an wie vielen Tagen des Monats der Kopfschmerz Migränecharakter haben muss und an wie vielen Tagen der Kopfschmerz eher einem Spannungskopfschmerz ähneln darf, um trotzdem noch für die Definition “chronische Migräne” zu qualifizieren. Inwieweit ein Medikamentenübergebrauch alleinig für die Chronifizierung einer primär episodischen Migräne verantwortlich ist und ob es sich bei der chronischen Migräne primär um eine Untergruppe der Migräneerkrankungen handelt, ist Gegenstand der aktuellen Forschung.


2005 ◽  
Vol 24 (03) ◽  
pp. 217-226 ◽  
Author(s):  
A. Frese ◽  
A. May ◽  
G. Sixt ◽  
A. Straube ◽  
S. Evers

ZusammenfassungDie Kopfschmerzklassifikation der International Headache Society unterscheidet in ihrem Kapitel 4 verschiedene idiopathische Kopfschmerzerkrankungen, die als selten gelten, aber als eigenständige Entitäten aufgefasst werden müssen. Zu diesen gehören der primäre stechende Kopfschmerz, der primäre Hustenkopfschmerz, der primäre Kopfschmerz bei körperlicher Anstrengung, der primäre Kopfschmerz bei sexueller Aktivität, der primäre schlafgebundene Kopfschmerz, der primäre Donnerschlagkopfschmerz, die Hemicrania continua und der neu aufgetretene tägliche Kopfschmerz. Es handelt sich um harmlose Erkrankungen mit einer guten Prognose, die aber die Lebensqualität der Betroffenen erheblich einschränken können. Aufgrund einer Analyse der publizierten Fallberichte und einem Expertenkonsens werden für diese Kopfschmerzerkrankungen Therapieempfehlungen gegeben, auch wenn große randomisierte, kontrollierte Studien nicht vorliegen. Die meisten dieser Erkrankungen sprechen neben einer spezifischen Therapie unter anderem auf Indometacin an.


2020 ◽  
Vol 79 (Suppl 1) ◽  
pp. 540.3-540
Author(s):  
A. Munir ◽  
C. Sheehy

Background:Corneal melt is a rare inflammatory disease of the peripheral cornea; it may lead to perforation of the globe and visual failure. Corneal melt can be a manifestation of systemic vasculitis in patients with RA and other conditions, such as cancer. Without early and aggressive treatment it may be associated with a poor visual outcome and a high mortality. It has been reported in patients with stable RA.Objectives:A case report in a patient with long standing but well controlled Rheumatoid Arthritis (RA) and metastatic disease.Methods:A 75 year old male with a background of sero positive Rheumatoid Arthritis for more than 10 years presented to the Eye Casualty with a two week history of a painful left red eye. His other medical history was significant for Stage IIB poorly differentiated cancer of the left lower lobe. Left lower lobectomy with a patch of diaphragm resected. Intratumoural lymphovascular invasion noted. He completed Adjuvant Carboplatin/Vinorelbine chemotherapy September, 2017. He had DVT proximal left leg 22ndof September, 2017. Follow up CT in 2018 demonstrated a right renal upper pole lesion for which he was awaiting biopsy with?metastatic lung disease vs primary renal carcinoma. His RA was well controlled on Methotrexate 10mg weekly. He had been treated by the ophthalmology team for left marginal Keratitis for the prior 2 months with steroid eye drops without significant improvement. On presentation to ED, he described sharp eye pain, waking him from the sleep, associated with watery discharge and photophobia. Examination showed corneal melt in left eye involving 25% of inferior portion of the cornea and spastic entropion with injecting eye lashes. He had no active joints and there were no other signs of vasculitis. CRP was 4.1. He had a negative ANA and ANCA; viral swabs were negative. He was admitted under the medical team. Intravenous Methyl Prednisolone was started. The patient felt better after 5 days of Methyl Prednisolone. Left temporary tarsorrhaphy was done by Ophthalmology. Cyclophosphamide was initiated after discussion with Oncologist pending the result of the renal biopsy. Patient was discharged after 5 days of admission in the hospitalResults:The renal biopsy was positive for metastatic Squamous cell carcinoma of lung. Cyclophosphamide was withdrawn and he was started on Carboplatin/Gemcitabine. The corneal melt improved with complete resolution of his visual symptoms.Conclusion:In this case, although the history of RA was felt by the ophthalmology team to be the most likely association with the corneal melt, we would argue the oncological diagnoses were likely the driving force behind the presentation.References:[1]Sule A, Balakrishnan C, Gaitonde S, Mittal G, Pathan E, Gokhale NS, et al. Rheumatoid corneal melt. Rheumatology (Oxford)2002;41:705–6.[2]S. Yano, K. Kondo, M. Yamaguchi et al., “Distribution and function of EGFR in human tissue and the effect of EGFR tyrosine kinase inhibition,” Anticancer Research, vol. 23, no. 5, pp. 3639–3650, 2003.Disclosure of Interests:None declared


2021 ◽  
Vol 7 (1) ◽  
pp. 39-62
Author(s):  
Lauren M. Pachman ◽  
Brian E. Nolan ◽  
Deidre DeRanieri ◽  
Amer M. Khojah

Abstract Purpose of review To identify clues to disease activity and discuss therapy options. Recent findings The diagnostic evaluation includes documenting symmetrical proximal muscle damage by exam and MRI, as well as elevated muscle enzymes—aldolase, creatine phosphokinase, LDH, and SGOT—which often normalize with a longer duration of untreated disease. Ultrasound identifies persistent, occult muscle inflammation. The myositis-specific antibodies (MSA) and myositis-associated antibodies (MAA) are associated with specific disease course variations. Anti-NXP-2 is found in younger children and is associated with calcinosis; anti-TIF-1γ+ juvenile dermatomyositis has a longer disease course. The diagnostic rash—involving the eyelids, hands, knees, face, and upper chest—is the most persistent symptom and is associated with microvascular compromise, reflected by loss of nailfold (periungual) end row capillaries. This loss is associated with decreased bioavailability of oral prednisone; the bioavailability of other orally administered medications should also be considered. At diagnosis, at least 3 days of intravenous methyl prednisolone may help control the HLA-restricted and type 1/2 interferon–driven inflammatory process. The requirement for avoidance of ultraviolet light exposure mandates vitamin D supplementation. Summary This often chronic illness targets the cardiovascular system; mortality has decreased from 30 to 1–2% with corticosteroids. New serological biomarkers indicate occult inflammation: ↑CXCL-10 predicts a longer disease course. Some biologic therapies appear promising.


Cephalalgia ◽  
2001 ◽  
Vol 21 (9) ◽  
pp. 906-910 ◽  
Author(s):  
JA Pareja ◽  
AB Caminero ◽  
E Franco ◽  
JL Casado ◽  
J Pascual ◽  
...  

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