Michael Saul Lundin
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Michael Saul Lundin has a total of 21 co-authors. Here are the top co-authors by number of shared publications:
Calvin Abro
Internal Medicine, Sparrow Hospital, Lansing, Michigan, USA
2 shared publicationsHeather Laird-Fick
Sparrow Hospital, Lansing, Michigan, USA
2 shared publicationsRajit Pahwa
Intensive Care and Neurointensive Care, Sparrow Hospital, Lansing, Michigan, USA
2 shared publicationsAbdullah Almohammadi
Hematology and Oncology, Michigan State University, Lansing, Michigan, USA
1 shared publicationAhmad Alratroot
Internal Medicine, Michigan State University, East Lansing, Michigan, USA
1 shared publicationAli Saeed
Hospital Medicine, Sparrow Hospital, Lansing, Michigan, USA
1 shared publication
Latest Publications
- 31 March 2020
- Published by BMJ in BMJ Case Reports
- Vol. 13 (3) , e231337
When thyroid labs do not add up, physicians should ask patients about biotin supplements
A 69-year-old woman with a remote history of Graves’ disease treated with radioactive iodine ablation, who was maintained on a stable dose of levothyroxine for 15 years, presented with abnormal and fluctuating thyroid function tests which were confusing. After extensive evaluation, no diagnosis could be made, and it became difficult to optimise the levothyroxine dose, until we became aware of the recently recognised biotin-induced lab interference. It was then noticed that her medication list included biotin 10 mg two times per day. After holding the biotin and repeating the thyroid function tests, the labs made more sense, and the patient was easily made euthyroid with appropriate dose adjustment. We also investigated our own laboratory, and identified the thyroid labs that are performed with biotin-containing assays and developed strategies to increase the awareness about this lab artefact in our clinics.
- 31 March 2020
- Published by BMJ in BMJ Case Reports
- Vol. 13 (3) , e231337
When thyroid labs do not add up, physicians should ask patients about biotin supplements
A 69-year-old woman with a remote history of Graves’ disease treated with radioactive iodine ablation, who was maintained on a stable dose of levothyroxine for 15 years, presented with abnormal and fluctuating thyroid function tests which were confusing. After extensive evaluation, no diagnosis could be made, and it became difficult to optimise the levothyroxine dose, until we became aware of the recently recognised biotin-induced lab interference. It was then noticed that her medication list included biotin 10 mg two times per day. After holding the biotin and repeating the thyroid function tests, the labs made more sense, and the patient was easily made euthyroid with appropriate dose adjustment. We also investigated our own laboratory, and identified the thyroid labs that are performed with biotin-containing assays and developed strategies to increase the awareness about this lab artefact in our clinics.
- 24 March 2020
- Published by BMJ in BMJ Case Reports
- Vol. 13 (3) , e231249
Syndrome of inappropriate antidiuretic hormone associated with eosinophilic granulomatosis and polyangiitis
A 62-year-old man presented with classic signs and symptoms of eosinophilic granulomatosis and polyangiitis (EGPA, also known as Churg-Strauss syndrome)—mononeuritis multiplex, palpable purpura, hypereosinophilia, positive P-ANCA (perinuclear anti-neutrophil cytoplasmic antibodies) developed diffuse alveolar haemorrhage. The patient had longstanding mild hyponatraemia, but developed moderate and symptomatic hyponatraemia characteristic of the syndrome of inappropriate antidiuretic hormone. The patient’s serum sodium returned to his baseline- mildly hyponatraemic, after initiation of treatment targeted towards EGPA.
- 24 March 2020
- Published by BMJ in BMJ Case Reports
- Vol. 13 (3) , e231249
Syndrome of inappropriate antidiuretic hormone associated with eosinophilic granulomatosis and polyangiitis
A 62-year-old man presented with classic signs and symptoms of eosinophilic granulomatosis and polyangiitis (EGPA, also known as Churg-Strauss syndrome)—mononeuritis multiplex, palpable purpura, hypereosinophilia, positive P-ANCA (perinuclear anti-neutrophil cytoplasmic antibodies) developed diffuse alveolar haemorrhage. The patient had longstanding mild hyponatraemia, but developed moderate and symptomatic hyponatraemia characteristic of the syndrome of inappropriate antidiuretic hormone. The patient’s serum sodium returned to his baseline- mildly hyponatraemic, after initiation of treatment targeted towards EGPA.
- Open Access
- 15 March 2020
- Published by BMJ in BMJ Case Reports
- Vol. 13 (3) , e231889
Lyme disease with erythema migrans presenting concurrently with optic nerve perineuritis and abducens nerve palsy
- 15 March 2020
- Published by BMJ in BMJ Case Reports
- Vol. 13 (3) , e231889
Open AccessLyme disease with erythema migrans presenting concurrently with optic nerve perineuritis and abducens nerve palsy
- Open Access
- 9 July 2019
- Published by BMJ in BMJ Case Reports
- Vol. 12 (7) , e231266
Petechial cimicosis in a patient on aspirin 81 mg, clopidogrel and warfarin
- 9 July 2019
- Published by BMJ in BMJ Case Reports
- Vol. 12 (7) , e231266
Open AccessPetechial cimicosis in a patient on aspirin 81 mg, clopidogrel and warfarin
- 8 June 2019
- Published by BMJ in BMJ Case Reports
- Vol. 12 (6) , e230431
Presumed superficial haemosiderosis presenting with subarachnoid haemorrhage
- 8 June 2019
- Published by BMJ in BMJ Case Reports
- Vol. 12 (6) , e230431
Presumed superficial haemosiderosis presenting with subarachnoid haemorrhage
- 6 May 2019
- Published by BMJ in BMJ Case Reports
- Vol. 12 (5) , e229423
Epistaxis and gross haematuria with severe thrombocytopaenia associated with influenza vaccination
Epistaxis may be attributed to many causes during the winter including dry mucous membranes from low indoor humidity from heating. However, epistaxis may also be due to thrombocytopaenia. Immune thrombocytopaenia purpura (ITP) is an autoimmune disorder causing thrombocytopaenia. Viral infections sometimes lead to ITP. Vaccines, predominantly the measles-mumps-rubella vaccine, have been associated with the development of ITP. There are several published case reports regarding influenza vaccine induced ITP. However, an association between ITP and influenza vaccination has not been firmly proven yet. We report the case of an adult with three episodes of epistaxis, each within 1 week of receiving a yearly influenza trivalent inactivated vaccine, the last episode being more severe and also featuring gross haematuria.
- 6 May 2019
- Published by BMJ in BMJ Case Reports
- Vol. 12 (5) , e229423
Epistaxis and gross haematuria with severe thrombocytopaenia associated with influenza vaccination
Epistaxis may be attributed to many causes during the winter including dry mucous membranes from low indoor humidity from heating. However, epistaxis may also be due to thrombocytopaenia. Immune thrombocytopaenia purpura (ITP) is an autoimmune disorder causing thrombocytopaenia. Viral infections sometimes lead to ITP. Vaccines, predominantly the measles-mumps-rubella vaccine, have been associated with the development of ITP. There are several published case reports regarding influenza vaccine induced ITP. However, an association between ITP and influenza vaccination has not been firmly proven yet. We report the case of an adult with three episodes of epistaxis, each within 1 week of receiving a yearly influenza trivalent inactivated vaccine, the last episode being more severe and also featuring gross haematuria.
- 31 March 2019
- Published by BMJ in BMJ Case Reports
- Vol. 12 (3) , e229835
Intra-abdominal follicular lymphoma masquerading as severe cardiopulmonary disease in a Vietnam War veteran exposed to agent orange
A 68-year-old Hispanic male US Army veteran with a medical history of chronic obstructive lung disease, undefined lung scarring, heart failure with preserved ejection fraction, obstructive sleep apnoea, obesity hypoventilation syndrome [on oxygen by nasal cannula 2–4 L, bilevel positive airway
- 31 March 2019
- Published by BMJ in BMJ Case Reports
- Vol. 12 (3) , e229835
Intra-abdominal follicular lymphoma masquerading as severe cardiopulmonary disease in a Vietnam War veteran exposed to agent orange
A 68-year-old Hispanic male US Army veteran with a medical history of chronic obstructive lung disease, undefined lung scarring, heart failure with preserved ejection fraction, obstructive sleep apnoea, obesity hypoventilation syndrome [on oxygen by nasal cannula 2–4 L, bilevel positive airway
- 13 February 2019
- Published by BMJ in BMJ Case Reports
- Vol. 12 (2) , e229116
Biceps tendon rupture associated with ciprofloxacin use for spontaneous bacterial peritonitis prophylaxis
A 70-year-old man with a medical history of alcoholic cirrhosis was sent from the skilled nursing facility to the emergency department with an abnormal haemoglobin value of 68 g/L (reference 125–165), compared with 103 g/L three weeks prior. On physical examination, the patient’s left
- 13 February 2019
- Published by BMJ in BMJ Case Reports
- Vol. 12 (2) , e229116
Biceps tendon rupture associated with ciprofloxacin use for spontaneous bacterial peritonitis prophylaxis
A 70-year-old man with a medical history of alcoholic cirrhosis was sent from the skilled nursing facility to the emergency department with an abnormal haemoglobin value of 68 g/L (reference 125–165), compared with 103 g/L three weeks prior. On physical examination, the patient’s left
- 7 February 2019
- Published by BMJ in BMJ Case Reports
- Vol. 12 (2)
One month of nitrous oxide abuse causing acute vitamin B 12 deficiency with severe neuropsychiatric symptoms
A 21-year-old university student studying abroad in the USA presented to the emergency department with double vision, lower extremity weakness with difficulty ambulating and other neuropsychiatric symptoms. MRI of the brain and spinal cord were normal. Vitamin B12 was 78 pg/mL (58 pmol/L, reference 211–911 pg/mL). The patient had been using nitrous oxide capsules used for whipped cream recharging, which she obtained from other students, a few times daily for a month for the purpose of anxiety relief. The patient was not a vegan or vegetarian. The patient was treated with intramuscular vitamin B12 repletion with partial resolution of neurologic symptoms and discharged on vitamin B12 supplementation.
- 7 February 2019
- Published by BMJ in BMJ Case Reports
- Vol. 12 (2)
One month of nitrous oxide abuse causing acute vitamin B 12 deficiency with severe neuropsychiatric symptoms
A 21-year-old university student studying abroad in the USA presented to the emergency department with double vision, lower extremity weakness with difficulty ambulating and other neuropsychiatric symptoms. MRI of the brain and spinal cord were normal. Vitamin B12 was 78 pg/mL (58 pmol/L, reference 211–911 pg/mL). The patient had been using nitrous oxide capsules used for whipped cream recharging, which she obtained from other students, a few times daily for a month for the purpose of anxiety relief. The patient was not a vegan or vegetarian. The patient was treated with intramuscular vitamin B12 repletion with partial resolution of neurologic symptoms and discharged on vitamin B12 supplementation.
- 19 July 2018
- Published by BMJ in BMJ Case Reports
- Vol. 2018
Lemierre’s syndrome and 2016 American College of Physician guidelines for pharyngitis: no to empiric coverage for bacterial pharyngitis. While no role for routine Fusobacterium PCR, keep suspicion for this pathogen
An 18-year-old woman presented to clinic with acute pharyngitis with 4/4 Centor criteria. Rapid streptococcal antigen test was negative. The patient, who was allergic to penicillin, was prescribed azithromycin. Ultimately, after 5 days and without any corticosteroids, she presented to the emergency department with 10/10 chest pain and was admitted to the intensive care unit. CT showed nodular lung disease and blood cultures on admission grew Fusobacterium, likely Fusobacterium nucleatum. She sustained two cardiac arrests, three tube thoracostomies, acute kidney injury requiring dialysis and ventilatory failure requiring tracheostomy. After 16 days in hospital and 18 days in long-term acute care, the patient was discharged home. It is unclear how much of this could have been prevented by prescribing an antimicrobial that had activity against Fusobacterium. When severe pharyngitis occurs, Fusobacterium needs to be considered as an underlying cause. In vitro macrolides have marginal activity against most anaerobes, such as this pathogen, and should be avoided.
- 19 July 2018
- Published by BMJ in BMJ Case Reports
- Vol. 2018
Lemierre’s syndrome and 2016 American College of Physician guidelines for pharyngitis: no to empiric coverage for bacterial pharyngitis. While no role for routine Fusobacterium PCR, keep suspicion for this pathogen
An 18-year-old woman presented to clinic with acute pharyngitis with 4/4 Centor criteria. Rapid streptococcal antigen test was negative. The patient, who was allergic to penicillin, was prescribed azithromycin. Ultimately, after 5 days and without any corticosteroids, she presented to the emergency department with 10/10 chest pain and was admitted to the intensive care unit. CT showed nodular lung disease and blood cultures on admission grew Fusobacterium, likely Fusobacterium nucleatum. She sustained two cardiac arrests, three tube thoracostomies, acute kidney injury requiring dialysis and ventilatory failure requiring tracheostomy. After 16 days in hospital and 18 days in long-term acute care, the patient was discharged home. It is unclear how much of this could have been prevented by prescribing an antimicrobial that had activity against Fusobacterium. When severe pharyngitis occurs, Fusobacterium needs to be considered as an underlying cause. In vitro macrolides have marginal activity against most anaerobes, such as this pathogen, and should be avoided.