7 research outputs found
The effect of prenatal diagnosis on antibiotic therapy in neonates with hypoplastic left heart syndrome : antibiotics in prenatally diagnosed patients with HLHS
Erythema ab igne as a side effect of working in a flower shop : case report and literature review
Introduction . Erythema ab igne (EAI) is a rare skin disease (since the common use of central heating) characterized by reticular, erythematous and hyperpigmented patches resulting from chronic exposure to infrared radiation. Although the condition is generally benign, chronic heat exposure can induce dysplasia and, rarely, squamous cell carcinoma. The pathogenesis of the disease is not yet fully understood.
Objective . Presentation of the diagnostic and therapeutic difficulties in a patient with EAI.
Case report. The patient had erythema ab igne that developed on the shins, due to the effect of a heating device used in the flower shop. The clinical presentation, differential diagnosis and available treatment options of the disease are described.
Conclusions . Erythema ab igne is a rare skin disease, but there is a need for special oncological observation of these patients
Chronic Inflammation as the Underlying Mechanism of the Development of Lung Diseases in Psoriasis: A Systematic Review
Psoriasis is a systemic inflammatory disease caused by dysfunctional interactions between the innate and adaptive immune responses. The systemic inflammation in psoriasis may be associated with the development of comorbidities, including lung diseases. In this review, we aimed to provide a summary of the evidence regarding the prevalence of lung diseases in patients with psoriasis and the potential underlying mechanisms. Twenty-three articles published between March 2010 and June 2021 were selected from 195 initially identified records. The findings are discussed in terms of the prevalence of asthma, chronic obstructive pulmonary disease, interstitial lung disease, obstructive sleep apnea, pulmonary hypertension, and sarcoidosis in psoriasis. A higher prevalence of lung diseases in psoriasis has been confirmed in asthma, chronic obstructive pulmonary disease, obstructive sleep apnea, and pulmonary hypertension. These conditions are important as they are previously unrecognized causes of morbidity and mortality in psoriasis. The development of lung diseases in patients with psoriasis can be explained by several mechanisms, including common risk factors, shared immune and molecular characteristics associated with chronic inflammation, as well as other mechanisms. Understanding the prevalence of lung diseases in psoriasis and their underlying mechanisms can help implement appropriate preventative and therapeutic strategies to address respiratory diseases in patients with psoriasis
Epidemiologia raka podstawnokomórkowego skóry – obserwacje jednego ośrodka
Introduction. Basal cell carcinoma is the most common malignant skin cancer. It is one of the so-called nonmelanoma skin cancers, the incidence of which has increased rapidly worldwide in recent years. Unfortunately, the National Cancer Registry in Poland does not classify basal cell skin cancer separately. Therefore, the precise data on the incidence in the population remain unknown. Work objective. Retrospective analysis of the incidence of basal cell carcinoma in NZOZ Med-Laser in Lublin in the years 2005 – 2015 depending on gender, age group, place of residence (urban-rural) and clinical form of the disease. Material and methodology. The data of NZOZ Med-Laser from the years 2005 - 2015 were used in the study. The data concern all patients with histopathologically diagnosed basal cell carcinoma, who during the period covered by the study were consulted either as outpatients or hospitalised in an institution providing dermatological services under contract with the National Health Fund (NFZ). Patients were divided into several groups depending on gender, age and place of residence. All groups were compared quantitatively and the results are shown in the figures below. Results. The data collected indicate that between 2005 and 2015 a total of 922 patients with basal cell carcinoma received dermatological treatment. Over the years, there has been a clear increase in the number of patients with basal cell carcinoma. The disease occurred mainly in people over 59 years of age, with the majority of women living in cities. The most common locations of the cancer are nose, cheeks, forehead and temporal area. Histopathologically, solidum, superficiale, exulceratum and pseudoadenoides were the most frequently diagnosed forms. Conclusions. Basal cell carcinoma of the skin is frequent in our society. Its incidence has been increasing in recent years. Therefore, action should be taken to create consistent international registries to gather reliable epidemiological data that would show the scale of the problem, which we are dealing with almost all over the world.Wprowadzenie. Rak podstawnokomorkowy jest najczęstszym nowotworem złośliwym skory. Należy do tzw. nieczerniakowych nowotworow skory, ktorych zachorowalność w ostatnich latach gwałtownie wzrosła na całym świecie. Niestety, Krajowy Rejestr Nowotworow w Polsce nie wyrożnia w swojej klasyfikacji osobno raka podstawnokomorkowego skory. W związku z tym dokładne dane dotyczące zachorowalności w populacji pozostają nieznane. Cel pracy. Analiza retrospektywna częstości występowania raka podstawnokomorkowego w NZOZ Med-Laser w Lublinie w latach 2005 - 2015 w zależności od płci, grupy wiekowej, miejsca zamieszkania (miasto-wieś) oraz postaci klinicznej choroby. Materiał i metodyka. W badaniu wykorzystano dane NZOZ Med-Laser z lat 2005 - 2015. Dane dotyczą wszystkich pacjentow z rozpoznanym histopatologicznie rakiem podstawnokomorkowym, ktorzy w okresie objętym badaniem byli konsultowani ambulatoryjnie lub hospitalizowani w placowce realizującej świadczenia dermatologiczne w ramach kontraktu z Narodowym Funduszem Zdrowia (NFZ). Pacjentow podzielono na kilka grup w zależności od płci, wieku oraz miejsca zamieszkania. Wszystkie grupy porownano ilościowo, a wyniki przedstawiono na rycinach. Wyniki. Zgromadzone dane wskazują, że w latach 2005 - 2015 ze świadczeń dermatologicznych skorzystało łącznie 922 pacjentow z rakiem podstawnokomorkowym. Na przestrzeni lat stwierdzono wyraźny wzrost liczby pacjentow z rakiem podstawnokomorkowym. Choroba występowała głownie u osob powyżej 59 roku życia, z przewagą kobiet mieszkających w miastach. Najczęstsze umiejscowienie nowotworu to nos, policzki, czoło oraz okolica skroniowa. Pod względem histopatologicznym najczęściej rozpoznawano postać solidum, superficiale, exulceratum i pseudoadenoides. Wnioski. Rak podstawnokomorkowy skory często występuje w naszym społeczeństwie. W ostatnich latach jego zachorowalność wzrasta. Dlatego należy podjąć działania, aby stworzyć spojne międzynarodowe rejestry, umożliwiające zebranie wiarygodnych danych epidemiologicznych, ktore pokazałyby skalę problemu, z jakim mamy do czynienia niemal na całym świecie
Assessment of Immune Cell Activation in Pemphigus
(1) Background: Pemphigus is a blistering autoimmune disease of the skin and/or mucous membranes, characterised by the presence of specific autoantibodies directed against structural proteins of the human skin. Recent reports indicate that new haematological parameters, termed Extended Inflammation Parameters (EIP), can be used to assess the activation of immune cells during active inflammation. These include parameters assessing both neutrophil activation (NEUT-RI, NEUT-GI) and the number of activated lymphocytes (RE-LYMP). The aim of this study was to investigate the relationship between changes in NEUT-RI, NEUT-GI and RE-LYMP and the disease activity in patients with pemphigus. (2) Results: The study involved 32 patients with diagnosed different types of pemphigus. Neutrophil activation parameters (NEUT-RI and NEUT-GI) and lymphocytes (RE-LYMP) were significantly higher in these patients compared to the parameters in healthy participants (respectively p = 0.0127, p = 0.0011 and p = 0.0033). The increased quantity of activated lymphocytes (RE-LYMP) also correlated significantly with the extent of skin and/or mucosal lesions in patients assessed by the PDAI scale (p < 0.02). (3) Conclusions: The NEUT-RI, NEUT-GI and RE-LYMP parameters proved to be appropriate markers of inflammation severity in pemphigus, also in relation to local lesions, which was not possible with the inflammation markers (CRP, ESR) used so far on a routine basis
Autosomal dominant polycystic kidney disease in children - single-center observational study
Diagnosis of Alport syndrome and thin basement membrane nephropathy in childhood
WSTĘP: Zespół Alporta (ZA) i choroba cienkich błon podstawnych (TBMN), jako genetycznie uwarunkowane glomerulopatie, są w wieku dziecięcym trudne do różnicowania i brak jest czynników prognostycznych odległych powikłań. Celem opracowania była analiza porównawcza przebiegu klinicznego i zmian histopatologicznych w biopsji nerki u dzieci z rozpoznanym ZA lub TBMN. MATERIAŁ I METODY: Grupę badaną stanowiło 53 dzieci (27 dziewczynek) w wieku 9,5 roku, leczonych w Uniwersyteckim Szpitalu Dziecięcym w Krakowie w latach 1988–2015 z powodu ZA (n = 25) lub TBMN (n = 28). Wynik biopsji nerki skorelowano w grupach z danymi klinicznymi z wykorzystaniem Statistica12(StatSoft). WYNIKI: Krwinkomocz rozpoznano u dzieci w wieku od 1 do 17 lat (mediana 6 lat), białkomocz u 14 dzieci z ZA (56%). Czas obserwacji przed wykonaniem biopsji był istotnie dłuższy w TBMN: 38 vs. 11 miesięcy w ZA (p = 0,01). U 11(39%) pacjentów z TBMN stwierdzono w biopsji przyrost mezangium. W ZA u 4(16%) pacjentów nie wykazano zmian morfologicznych. W analizie regresji wieloczynnikowej najsilniejszym parametrem patomorfologicznym, warunkującym występowanie białkomoczu, była nieregularna grubość błon podstawnych (R2 = 0,56, p = 0,011). W leczeniu stosowano ACEI u 14 dzieci z białkomoczem, prednizon u 8, cyklosporynę A u 8, pulsy methylprednizolonu u 2. U dwóch chłopców rozwinęła się schyłkowa niewydolność nerek przed 18 r.ż. U 2 pacjentów z rozpoznaniem wstępnym TBMN wystąpił w dalszym przebiegu choroby białkomocz. WNIOSKI: U dzieci z ZA i TBMN czynnikami złej prognozy są białkomocz z nieregularnością błon podstawnych kłębuszka. Obecność izolowanego krwinkomoczu i ścieńczenia błon podstawnych nie wyklucza złego rokowania. Wczesne wykonywanie biopsji nerki u młodych pacjentów z izolowanym krwinkomoczem nie jest miarodajne. Rekomenduje się zatem wprowadzenie do diagnostyki badań genetycznych umożliwiających wczesne rozpoznanie.INTRODUCTION: The Alport syndrome (AS) and thin basement membrane nephropathy (TBMN) are glomerulopathies of genetic origin difficult to differentiate, with no predictors of a long term outcome. The aim of the study was to analyze clinical data regarding kidney histopathology in children with AS and TBMN. MATERIAL I METHODS: The study group consisted of 53 children (27 girls) aged 9.5 years, treated for AS (n = 25) or TBMN (n = 28) at University Children's Hospital of Cracow between 1988–2015. The kidney biopsy result was correlated with clinical data in both groups using Statistica12 (Statsoft). RESULTS: Hematuria was diagnosed in all the children at the age of 1–17 (median 6 years) and proteinuria in 14 patients with AS (56%). The follow-up time before biopsy was longer in TBMN – 38 vs. 11 months (p = 0.01). In 11 (39%) TBMN patients mesangial proliferation was observed. Among the AS patients in 4 cases (16%) no kidney pathology was found. Multiple regression analysis indicated an irregular basement membrane structure as the most significant predictor for proteinuria (R2 = 0.56, p = 0.011). Therapy with ACEI was introduced in 14 patients with proteinuria, prednisone in 8 patients, cyclosporine A in 8 and methylprednisolone pulses in 2. Two boys progressed to end stage renal failure before the age of 18 years. Two patients with TBMN developed proteinuria in later follow-ups. CONCLUSIONS: Proteinuria and irregularity of basement membrane in children with AS and TBMN are predictors of poor prognosis. Hematuria and thinning of basal membrane do not ensure benign follow-up. Early kidney biopsy in young children with isolated hematuria seems to be not useful. Intorduction of genetical testing is needed for early diagnosig instead