A Case Report of Prophylactic Hemin Treatments in the Management of Patients with Life-Threatening Attacks of Acute Intermittent Porphyria.

Blood ◽  
2005 ◽  
Vol 106 (11) ◽  
pp. 3757-3757
Author(s):  
Richard E. Mills

Abstract Background The acute porphyrias are a group of 4 genetic disorders resulting from a deficiency in a specific enzyme of the heme biosynthetic pathway (1). Without prompt treatment, these disorders can cause acute life-threatening attacks of neurovisceral symptoms, the most common being abdominal pain, nausea, vomiting, mental symptoms, paresis, and tachycardia (1). Frequent, non cyclic attacks can sometimes be prevented with weekly or bi-weekly infusions of hemin (2). Case Report A 25-year-old female was initially diagnosed with acute intermittent porphyria (AIP) at 16 years of age. Her initial presenting symptoms included acute abdominal pain, nausea, vomiting, and a seizure. The patient was subsequently diagnosed by the evidence of elevated urinary porphobilinogen levels. She was initially treated with fluids (D5W) and then with hemin (313mg) for 3 days. The patient is a smoker and occasionally drinks alcohol. At 22 years of age, she was hospitalized for her fifth acute attack of AIP and received treatment with fluids and a course of hemin (313mg) for three days. Her condition improved and she was discharged. Two days later, her condition deteriorated and she was readmitted. She developed pneumonia, hyponatremia, seizures, and mental-status changes. The patient became tetraplegic and developed progressive respiratory failure requiring ventilatory support. She remained comatose for a period of 48 hours. Diagnostic studies included a noncontrast CT scan of the abdomen/pelvis which was unremarkable and EMG nerve conduction studies demonstrating polyneuropathies. Treatment included D5W, then increased to D10W. Following placement of a PICC line, hemin (313mg) was administered daily. Hemin therapy was continued daily for a period of three weeks and then stepped down to twice/week (313mg) every week in a prophylactic fashion. Her hospital course was prolonged as a result of the following: MRSA, VRE, superventricular tachycardia, arrhythmias, fungal infection, pulmonary infection and a clot in her right subclavian vein. She also experienced intermittent mental status changes. She was discharged to a rehabilitation center following her 11 month hospital stay. Upon discharge, her paresis had resolved, although a loss of motor function persisted. The patient was discharged with hemin therapy for prophylaxis twice/week (313mg with albumin 25%) via a portacath. She has experienced one acute attack of AIP during her course of prophylaxis during a three year period. The patient’s current medical status is that she is alert and oriented with the ability to work from home utilizing a telephone and computer. She remains wheel chair bound with loss of motor function. Discussion: Delay of treatment, and the delay in treating the pathophysiology of the disease itself can cause life-threatening attacks. Acute intermittent Porphyria is a disease that is challenging to manage in this particular patient. It is important for patients to recognize the triggers that exacerbate an attack. This particular patient still has 2 precipitating factors for acute attacks, smoking and alcohol. The prophylactic dosing regimen for this patient has been effective despite the presence of these precipitating factors. This case report is an example of the effectiveness of hemin therapy in the prevention of acute attacks of AIP.

Blood ◽  
2005 ◽  
Vol 106 (11) ◽  
pp. 3771-3771
Author(s):  
Rene Rothstein-Rubin

Abstract Background Acute intermittent porphyria (AIP), is one of the acute porphyrias resulting from deficient activity of a distinct enzyme in the heme biosynthetic pathway. Porphobilinogen deaminase, is the enzyme in AIP with approximately 50% activity1. This predisposes individuals to factors exacerbating the disease, including drugs inducing heme synthesis and cytochrome P450 enzymes, steroids, dieting, smoking, stress, and infection. Clinically, AIP is characterized by visceral, autonomic, peripheral, and CNS involvement, leading to varying degrees of intermittent and life-threatening symptoms. Despite avoidance of these factors, frequent attacks may persist due to unidentified modifier genes or environmental/endogenous factors1. Recurrent noncyclic attacks may be prevented by weekly or biweekly infusions of hemin2. Objective To report the results of the prevention of acute life-threatening attacks of AIP by a multidisciplinary team leading to a 50–100% decrease in patient hospitalizations. Methods Three patients were diagnosed with AIP on the biochemical basis of increased urinary porphobilinogen and aminolevulinic acid levels. All patients required hospitalization over 3–5 years due to severe abdominal pain and inability to maintain caloric intake and hydration. Due to recurrent attacks, hemin 313 mg was initiated on a prophylactic basis and frequency of administration was dependent on activity of their disease. All 3 patients served as their own control and the outcome of hemin prophylaxis was measured by patient symptoms, narcotic requirements, physical examination, and hospitalizations. Results Three patients (1 female, 2 male) with a mean age of 58 years had recurrent attacks of AIP. Patient #1 was hospitalized monthly over 5 years and received hemin for 10 days during acute attacks. Hemin infusions 1/month was initiated, and hospitalizations decreased by 50% until discontinued due to severe cardiomyopathy (unknown if related to porphyria). She expired in hospice care. Patient #2 was classified as a drug seeker for 3 years. After diagnosis, he was hospitalized almost monthly for 3–5 days during acute attacks over 2–3 years. Hemin was infused 1/month and symptoms persisted. Infusions were increased to 2/month. Symptoms and narcotic requirements have decreased and he has not been hospitalized. Patient #3 experienced acute attacks during stress, increasing due to business travel abroad. He was hospitalized 4 times in 3 years. As a nurse, he self-administers 1/month and in the office approximately every 2–3/months. 2 of 3 patients experienced phlebitis during infusions and receive via a portacath with no further adverse events. 2 of 3 patients have not required hospitalizations for acute attacks, symptoms have decreased and/or resolved, as well as narcotic requirements. Conclusions The experience in management of these three patients demonstrates the safety and effectiveness of hemin as a prophylactic agent in AIP. Most patients will require treatment 1–2 times/month and can avoid painful crisis and hospitalizations. PATIENT DATA, TREATMENT, AND RESULTS Patient Age Sex Yr Diagnosis Presenting Sxs Txment Frequency Hospitalizations 1 66 F 1990 Abdominal Pain, Difficulty Urinating 1 month/5yrs 50% ↓ 2 52 M 1996 Abdominal Pain, Neuropathic Sxs 2 month/2 yrs 100%↓ 3 56 M 2002 Abdominal Pain, Paresthesias 1 month/8 mos 100%↓


2014 ◽  
Vol 2014 ◽  
pp. 1-4
Author(s):  
Rania Elkhatib ◽  
Modupe Idowu ◽  
Gregory S. Brown ◽  
Yasmeen M. Jaber ◽  
Matthew B. Reid ◽  
...  

Acute intermittent porphyria (AIP) is an autosomal dominant genetic defect in heme synthesis. Patients with this illness can have episodic life-threatening attacks characterized by abdominal pain, neurological deficits, and psychiatric symptoms. Feigning this illness has not been reported in the English language literature to date. Here, we report on a patient who presented to the hospital with an acute attack of porphyria requesting opiates. Diligent assessment of extensive prior treatment records revealed thirteen negative tests for AIP.


JMS SKIMS ◽  
2019 ◽  
Vol 21 (2) ◽  
pp. 117-119
Author(s):  
Munir Ahmad Wani ◽  
Mubarak Ahmad Shan ◽  
Syed Muzamil Andrabi ◽  
Ajaz Ahmad Malik

Gallstone ileus is an uncommon and often life-threatening complication of cholelithiasis. In this case report, we discuss a difficult diagnostic case of gallstone ileus presenting as small gut obstruction with ischemia. A 56-year-old female presented with abdominal pain and vomiting. A CT scan was performed and showed an evolving bowel obstruction with features of gut ischemia with pneumobilia although no frank hyper density suggestive of a gallstone was noted. The patient underwent emergency surgery and a 60 mm obstructing calculus was removed from the patient's jejunum, with a formal tube cholecystostomy. JMS 2018: 21 (2):117-119


F1000Research ◽  
2021 ◽  
Vol 10 ◽  
pp. 1219
Author(s):  
Prashant Pant ◽  
Oshan Shrestha ◽  
Pawan Budhathoki ◽  
Nebula Devkota ◽  
Prabin Kumar Giri ◽  
...  

Ludwig’s angina (LA) is a rapidly spreading and potentially life-threatening infection having an odontogenic infection as the most common source. It involves the floor of the mouth and neck. Modernization in medical care has made this entity rare and of low mortality at the present but it is still feared as a lethal entity due to rapidly progressive airway obstruction that follows. Here we report a case of a 15-year-old male who suffered from LA. Presenting symptoms and findings of the examination helped in the clinical diagnosis. Immediate intubation, use of broad-spectrum antibiotics, and treatment of complications aided the patient’s recovery. LA should be considered for differential diagnosis in the case of neck swelling especially in those having a history of poor oral hygiene and recent dental procedures. Management of LA and its complications should always involve doctors from multiple disciplines.


Neurosurgery ◽  
2010 ◽  
Vol 67 (6) ◽  
pp. E1845-E1851 ◽  
Author(s):  
David S Xu ◽  
Asad A Usman ◽  
Michael C Hurley ◽  
Christopher S Eddleman ◽  
Bernard R Bendok

Abstract BACKGROUND AND IMPORTANCE: Vein of Galen aneurysmal malformations (VGAMs) arise from persistent arteriovenous shunting from primitive choroidal vessels into the median prosencephalic vein of Markowski, the embryonic precursor of the vein of Galen. VGAMs rarely present past infancy, and their natural history in adults is unknown. We report the first case of a familial-associated VGAM in an asymptomatic adult female patient. The clinical features of this case are presented alongside a systematic review of the literature on adult VGAM cases to assess the natural history, clinical management, and genetic basis of this rare neurovascular lesion. CLINICAL PRESENTATION: A previously healthy 44-year-old woman with a family history of a VGAM in a stillborn presented with an 8-week onset of dizziness and vertigo that spontaneously resolved. Time-resolved magnetic resonance angiography identified a choroidal VGAM. No intervention was undertaken at this time because of the patient's asymptomatic status after 9 months of follow-up. CONCLUSION: Based on our review of the literature, this is the first case report of a familial-associated VGAM in an adult patient and suggests that VGAM development can be genetically linked. Of 15 adult VGAM cases previously reported, all patients were either symptomatic or treated, thus precluding determination of VGAM natural history in adults. Patient outcomes correlated with the severity of presenting symptoms, which ranged from asymptomatic to immediately life-threatening. We hypothesize that self-selection may render VGAMs to be more benign for them to persist past childhood. Further investigation of the molecular biology underlying VGAM development is warranted.


2020 ◽  
pp. 1-3
Author(s):  
Bhuvana Lakshmi Sundararajan ◽  
Siddartha Gowthaman ◽  
Arul Kumar ◽  
Ramanathan M

INTRODUCTION: Pica is common in patients with developmental disabilities and can be life-threatening. It is important to identify pica and manage it appropriately. CASE REPORT:A 19-year-old male presented with history of abdominal pain and vomiting for two days.On imaging he was found to have multiple foreign bodies within the small and large bowel.After trial of conservative management,he was taken up for exploratory laparotomy. He was found to have trichobezoar and lithobezoar obstructing the bowel at terminal ileum.Bezoars when removed via enterotomy. DISCUSSION: Bezoars are conglomerates of non-absorbable food or fibre formed in the alimentary tract.Trichobezoar forms following ingestion of hair and usually leads to gastric outlet obstruction.Lithobezoar refers to the accumulation of stones in the GIT. Reports of colonic lithobezoar are rare. Pica is the persistent ingestion of non-nutritive substances beyond a developmentally inappropriate age. Patients should be referred to a psychologist/behaviour analyst and caregivers should also be educated


2021 ◽  
pp. 000313482110474
Author(s):  
Yeahwa Hong ◽  
Christopher Staniorski ◽  
Dean Pollack ◽  
Steven Evans

Esophageal and gastric mucosal injuries are well-documented adverse effects of doxycycline leading to odynophagia, chest pain, and abdominal pain. There are no clear diagnostic criteria for such adverse effects; hence, the diagnosis depends heavily on thorough history. There is a paucity of literature describing life-threatening complications from doxycycline-induced mucosal injury, such as hemorrhage and perforation. We present the first case report describing a gastric perforation from doxycycline use.


Author(s):  
André Luiz Santos Rodrigues ◽  
Marcelino Ferreira Lobato ◽  
Carla Andrea Ribeiro Braga ◽  
Lucas Crociati Meguins ◽  
Daniel Felgueiras Rolo

INTRODUCTION: Gallbladder empyema is a serious complication of acute cholecystitis being peritonitis and sepsis it's main clinical consequences. Organ giant volume is rare specially with no relevant symptoms. CASE REPORT: Man 56-year-old with mild abdominal pain on the right hypochondrium, palpable gallbladder and ultrasound images revealing cholelithiasis. At surgery, there was a giant dilatation of the gallbladder with 580 mL of purulent bile. Cholecystectomy was carried out without post-operative complications. CONCLUSION: Early cholecystectomy should always be realized in patients presenting symptoms of gallbladder empyema no matter the size of it.


2020 ◽  
Vol 3 (2) ◽  
pp. 1-7
Author(s):  
Volkan Sarper Erkci

Plastic bronchitis (PB) is a rare disease characterized by the presence of mucofibrinous plugs which may occlude and conform the shape of tracheobronchial tree. These casts are exteremely cohesive. Most common presenting symptoms include cough, fever and dyspnea and if the cohesive casts occlude the airway totally life-threatening complications and even death may occur. The aim of treatment is to remove the casts and adress the symptoms. In this study a 6-year-old boy with PB is presented. In addition to medical treatment obstructing casts were removed via rigid bronchoscope. It is aimed to review the clinical and radiographic features and choices of treatment in this disease.


2016 ◽  
Vol 35 (3) ◽  
pp. 298-300
Author(s):  
Deepak Dwivedi ◽  
Jyoti Singh

Splenic involvement is frequently observed during malarial episode. This involvement may vary from simple asymptomatic splenic enlargement to serious complication such as hematoma, rupture, or infarction. Very few cases of splenic infarction in paediatric patients are reported in literature. This case report suggests that if a patient with malaria is complaining of left upper quadrant abdominal pain, and/or enlarging tender splenomegaly is observed during treatment, splenic infarct should be suspected and managed accordingly to avoid further life-threatening complications.J Nepal Paediatr Soc 2015;35(3):298-300


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