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040 _aAIKTC-KRRC
_cAIKTC-KRRC
100 _927143
_aGladwin, Evangeline
245 _aExploring the clinical spectrum and individualized drug therapy in pemphigus vulgar is
_b: a case series
250 _aVol.16(7)
260 _aBhopal
_bInnovare Academic Sciences Pvt Ltd
_c2024
300 _a54-57p.
520 _aPemphigus Vulgaris (PV) is a rare, chronic, life-threatening immunopathogenic disease that is characterized by flaccid, easily ruptured intraepithelial bullae, mostly found on the skin and mucous membranes. Attempting to keep the treatment plan of this potentially deadly disorder in primary focus, we have observed five patients with Pemphigus vulgaris. All patients have been presented with oral lesions or ulcers resulting in difficulty in swallowing. Patient one had a family history of the disease, while the other patients did not present any family history. All five patients had diverse ways of dealing with the disease before getting hospitalized. Microcytic anaemia and hypoalbuminemia have been found in all of them. Patients 1 and 3 had leucocytosis, while patient three had platelets in clumps with Hypercobalaminemia and the presence of ketone bodies in urine analysis. The Desmoglein I and Desmoglein III Antibody along with Punch biopsy results, confirmed the diagnosis. All patients were given systemic corticosteroids on hospitalization, but the case series observed variations in the dosages emphasizing individualized drug therapy. Some developed psychological impairment, some had generalized headaches or cardiac impairment, while ophthalmic involvement was seen in the other patients. Healthcare providers should do close monitoring while providing individualized drug therapy to prevent any systemic involvement and further complications.
650 0 _94639
_aPHARMACEUTICS
700 _927250
_aShah, Priyanshi
773 0 _tInternational journal of pharmacy and pharmaceutical science
_dBhopal Innovare Academic Sciences Pvt Ltd
_x2656-0097
856 _uhttps://journals.innovareacademics.in/index.php/ijpps/article/view/51143
_yClick here
942 _2ddc
_cAR