/var/www/perpustakaan972/lib/SearchEngine/DefaultEngine.php:610 "Search Engine Debug 🔎 🪲"
Engine Type ⚙️: "SLiMS\SearchEngine\DefaultEngine"
SQL ⚙️: array:2 [ "count" => "select count(distinct b.biblio_id) from biblio as b left join mst_publisher as mp on b.publisher_id=mp.publisher_id left join mst_place as mpl on b.publish_place_id=mpl.place_id where b.opac_hide=0 and (b.biblio_id in(select bt.biblio_id from biblio_topic as bt left join mst_topic as mt on bt.topic_id=mt.topic_id where mt.topic like ?))" "query" => "select b.biblio_id, b.title, b.image, b.isbn_issn, b.publish_year, mp.publisher_name as `publisher`, mpl.place_name as `publish_place`, b.labels, b.input_date, b.edition, b.collation, b.series_title, b.call_number from biblio as b left join mst_publisher as mp on b.publisher_id=mp.publisher_id left join mst_place as mpl on b.publish_place_id=mpl.place_id where b.opac_hide=0 and (b.biblio_id in(select bt.biblio_id from biblio_topic as bt left join mst_topic as mt on bt.topic_id=mt.topic_id where mt.topic like ?)) order by b.last_update desc limit 10 offset 0" ]
Bind Value ⚒️: array:1 [ 0 => "%pemphigus%" ]
Two cases of pemphigus foliaceus in a 31-years old man and a 33-years old woman, treated in the outpatient department of the Department of Dermato-venereology Palembang General Hospital, are reported. The cases were initially diagnosed as seborrhoic dermatitis and discoid lupus erythematosus as the lesions were located on the face and there were no obvious blisters. The disease is a rare entity…
Two cases of pemphigus foliaceus in a 31-years old man and a 33-years old woman, treated in the outpatient department of the Department of Dermato-venereology Palembang General Hospital, are reported. The cases were initially diagnosed as seborrhoic dermatitis and discoid lupus erythematosus as the lesions were located on the face and there were no obvious blisters. The disease is a rare entity…
Hailey-Hailey disease (familial benign chronic pemphigs) is a rate herediatary disease with varied clinical morphology. We report a case of Hailey-Hailey disease which at first was treated as recurrent dermatophytosis. The diagnosis was confirmed as Hailey-Hailey disease by histopathology and direct immunofluorescence.