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The diet can be cumbersome; failure to comply with the diet may cause relapse.
It is well documented that watching other people smoke may cause relapse in quitters.
Persistent disease may cause relapse, although it has also been hypothesized that disease contamination in infused stem cells may also contribute to recurrence.
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However, persistent activation and accumulation of autoreactive LLPCs in the bone marrow may cause relapses in patient with SLE even after long periods of clinical inactivity [ 6, 27].
B. miyamotoi infection may cause relapsing fever and Lyme disease like symptoms throughout the Holarctic region of the world because of the widespread prevalence of this pathogen in its ixodid tick vectors.
The widespread distribution of P. ovale in Southeast Asia affects the choice of appropriate drugs for malaria chemoprophylaxis in travelers, since most currently used regimens are not effective against the dormant liver stages of P. ovale and P. vivax, which may cause relapses several months after the primary infection (3).
Moreover, the majority of cells that survive, arrest and extravasate in lymph nodes, lungs, liver and bone marrow will remain dormant for many years and may never cause relapse of cancer.
Severe gastrointestinal disease can be observed in congenital infections [ 1], in children with AIDS, or in children receiving immunosuppressive therapy post-transplantation. CMV may also cause relapses of intestinal disease in infants affected by inflammatory bowel diseases [ 3].
However, a number of patients with CML die due to ABL mutation-related drug resistance and blast crisis because IM does not kill leukemia stem cells (LSCs), which persist in a majority of patients and may cause disease relapse, and clinical resistance may develop predominantly due to point mutations in the ABL kinase domain [ 2].
Look out for those situations that may cause you to relapse into anorexic habits.
In case of P. vivax and P. ovale infections, dormant liver stages (hypnozoites) may cause infections (so-called relapses) weeks to months after adequate prophylaxis or effective blood-stage therapy of a primary infection.
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