Could attacks of abdominal pain in cases of acute intermittent porphyria be due to intestinal angina?

2000 ◽  
Vol 247 (3) ◽  
pp. 407-409 ◽  
Author(s):  
F. Lithner
2017 ◽  
Vol 4 ◽  
pp. 2329048X1773617 ◽  
Author(s):  
V. R. Souza Júnior ◽  
V. M. V. Lemos ◽  
I. M. L. Feitosa ◽  
R. Florencio ◽  
C. W. B. Correia ◽  
...  

A 16-year-old female who was attended as an outpatient reported localized, acute abdominal pain with vomiting, symmetrical motor weakness, and burning sensation in both arms and legs. Her medical history showed irrational behavior, repeated admissions at the emergency units of many other reference hospitals, where she had been investigated for celiac disease and treated with analgesics for pain events. Her clinical condition remained unchanged despite the use of many oral analgesics. In those admissions, she showed dysautonomia, vomiting, and abdominal pain. Diagnosis investigation disclosed a notable serum hyponatremia (133.7 mEq/L). She was referred for endoscopy and the histopathological lesion of the antrum in the stomach did not show neoplastic lesions. Colonoscopy, pelvic magnetic resonance imaging (MRI), total abdominal computed tomography, and video laparoscopy were without significant abnormalities. Suspicion of acute intermittent porphyria was confirmed by quantitative urine porphobilinogen-level tests and genetic analysis. Patient was successfully treated with intravenous infusion of glucose and hemin therapy.


2020 ◽  
Vol 20 (6) ◽  
pp. 486-488
Author(s):  
Grace Swart ◽  
Su San Lim ◽  
Martin Jude

Acute intermittent porphyria is a rare genetic condition in which disrupted haem synthesis causes overproduction of porphyrin precursors. Occasionally, it is associated with posterior reversible encephalopathy syndrome (PRES), presenting with headache, confusion, seizures and visual disturbance. We describe a patient with acute intermittent porphyria who presented with seizures and PRES, and who had previous unexplained severe abdominal pain. Acute intermittent porphyria should be considered as a possible cause of PRES, especially in those with unexplained abdominal pain, since delays in its diagnosis can result in permanent complications.


2002 ◽  
Vol 252 (3) ◽  
pp. 265-270 ◽  
Author(s):  
C. Andersson ◽  
A. Nilsson ◽  
T. Backstrom

2019 ◽  
Vol 11 (1) ◽  
pp. e2019018 ◽  
Author(s):  
Kanjaksha Ghosh ◽  
Kanchan Mishra ◽  
Avani Shah ◽  
Parizad Patel ◽  
Shrimati Shetty

An otherwise healthy male child of 9 years presented with paroxysmal fever and diffuse abdominal pain along with loss of appetite and nausea lasting for 3-4days every 4-6 weeks for last 2 years. He also has stretchable skin and hypermobile joint which he inherited from his mother who never suffered any paroxysmal attack of the kind.  Work up for acute intermittent porphyria, lead poisoning and familial mediterranean fever was negative. A novel harmful sequence change in NLRP12 gene was detected and a diagnosis of NLRP12 associated autoinflammatory syndrome was made. This sequence change with disease has not yet been reported in the literature and is the first such case of NLRP12 related autoinflammatory syndrome from India.


Blood ◽  
2005 ◽  
Vol 106 (11) ◽  
pp. 3759-3759
Author(s):  
Raymond J. Jensen

Abstract Background: Acute Intermittent Porphyria (AIP) is one of the genetic disorders of heme biosynthesis characterized by acute life-threatening attacks of nonspecific neurologic symptoms (1). Gastrointestinal symptoms include abdominal pain, nausea, and vomiting. Neurologic symptoms include pain in extremities, back, chest, or head. Little has been written on pregnancy and porphyria. Neilson and Neilson (1985) (2) reviewed literature for the outcome of pregnancy in porphyria and was able to gather data on 76 pregnancies occurring among 40 patients. They report AIP attacks in 95% of patients. Case Report: The subject is a 35 year-old female, who underwent 2 previous pregnancies. In each pregnancy, she experienced acute episodes of AIP and received intravenous (IV) hematin. The patient was diagnosed in 1995 and became pregnant in 1998. During pregnancy # 1, at 23 wks gestation, the patient presented to the ER and was admitted with AIP. Symptoms included severe abdominal pain and nausea and vomiting. She received 165mg of hematin IV daily 3 days and then was discharged when symptoms resolved. At 25 wks gestation, the patient was admitted for AIP and received 4 doses of hematin. The patient was discharged after 4 days, when symptoms abated. At 32 wks gestation, the patient was admitted for the third time with AIP and given 3 doses of hematin. Her symptoms were included acute abdominal pain, back pain and uncontrolled nausea and vomiting. The patient received a total of 13 doses of hematin during her 4 admissions. The baby was delivered vaginally at term with normal APGAR scores and normal birth weight. The patient was negative for hepatitis and HIV. During pregnancy # 2, the patient presented to the ER at 26 wks gestation. Symptoms included severe abdominal and back pain, uncontrolled nausea and vomiting and upper extremity weakness. Patient received 220mg of hematin and was discharged later that day when symptoms subsided. The patient returned to the ER at 28 wks gestation with complaints of severe abdominal pain, back pain, nausea and vomiting. Patient again received 220mg of hematin but was admitted to the hospital for IV hematin once a day for three days. At 30 wks gestation, the patient presented to the ER with acute abdominal pain, nausea and vomiting and was given 220mg and was discharged later that day. At 32 wks gestation, the patient entered the ER with upper and lower abdominal pain. She received 220 mg of hematin and later was discharged. The patient delivered a healthy baby at 35 weeks gestation. The baby had a normal APGAR and normal birth weight. During her last trimester, the patient received a total of 6 doses of hematin during her second pregnancy. The patient continues to be negative for hepatitis and HIV. Conclusion: Hematin is safe for pregnant women and the fetus. Hematin effectively treated symptoms of AIP. Hematin Dosing Total # Hematin Doses During Pregnancy Dosing/Hematin Infusion Symptoms Pregnancy # 1 13 165 mg Abdominal and Back Pain, Nausea, Vomiting Pregnancy # 2 6 220 mg Abdominal and Back Pain, Nausea, Vomiting Baby Weight Milestones 2 Weeks Check Up 2 Months Check Up 4 Months Check Up Baby 1 6.3 lbs 9.0 lbs 12.0 lbs Baby 2 6.5 lbs 9.1 lbs 11.2 lbs


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.


2013 ◽  
Vol 4 (4) ◽  
pp. 93-95
Author(s):  
Dmitry Vladimirovich Pechkurov ◽  
Evgeniya Nikolayevna Voronina ◽  
Yuliya Evgenyevna Allenova

Abdominal pain is often occur in practice of the pediatrician and gastroenterologist. Recurrent, intense, intractable abdominal pain for several years should be a symptom of anxiety. In this article, we present a case of long-term recurrent abdominal pain in a girl, accompanied by neurological symptoms, as a symptom of a rare disease - acute intermittent porphyria. Acute intermittent porphyria - inherited by dominant type disease characterized by lesions of the peripheral and central nervous system, the most frequent symptom of which is pain in the abdomen. Abdominal pain with this disease are recurrent paroxysmal and may be localized in different parts of the stomach, leading to the setting false diagnoses, multiple hospitalizations and unjustified surgical procedures.


2014 ◽  
Vol 25 (2) ◽  
pp. 93-95
Author(s):  
Md Ferdous ◽  
Abu Syeed ◽  
Md Gofranul Hoque

A 22 year young boy presented with recurrent abdominal pain, generalized weakness & wasting with hypertension in Medicine ward CMCH. Subsequently he was diagnosed as a case of Acute Intermittent Porphyria (AIP). Though not common, any patient with unexplained abdominal crisis specially young with any peripheral or central nervous system dysfunction should raise the clinician's suspicion of being porphyric patient as prompt management can relieve the patient from progressive neurological damage and disability. DOI: http://dx.doi.org/10.3329/medtoday.v25i2.17929 Medicine Today 2013 Vol.25(2): 93-95


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%↓


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