A patient hailing from Delhi presents with fever, arthralgia, and extensive petechial rash for 3 days. Lab investigations revealed a hemoglobin of 9 g/ dL, a white blood cell count of 9000 cells/mm3, a platelet count of 20000 cells/mm3, and a prolonged bleeding time. The clotting time was normal. What is the most likely diagnosis?
Patient: fever, joint pain, rash. Recent history of mosquito bite. Most likely diagnosis in urban area?
Recrudescences are commonly seen in which type of malaria:
A previously healthy child has sudden onset of red spots on body. There is a history of a preceding viral infection 1-4 weeks before the onset.
Which of the following statements regarding diagnosis of malaria are true?
Patient on anti-TB drugs develops tender nodules on shins. Most likely diagnosis is:
Most common precipitant of contact dermatitis is?
Which of the following drug classes is commonly implicated in causing Stevens-Johnson syndrome?
Cutis marmorata occurs due to exposure to –
Which of the following conditions is characterized by the sign of the groove?
Explanation: Dengue - The combination of **fever, arthralgia, extensive petechial rash**, and severe **thrombocytopenia** (platelet count 20,000/mm³) with **prolonged bleeding time** is highly characteristic of severe dengue infection, especially in an endemic area like Delhi [1]. - While leukocytosis (WBC 9000/mm³) is not typical for dengue (usually causes leukopenia), the other features strongly point to dengue hemorrhagic fever [1]. *Malaria* - Typically presents with **intermittent high fever**, chills, and sweats. While it can cause some thrombocytopenia and anemia, the **extensive petechial rash** is not a characteristic feature. - **Thrombocytopenia** in malaria is usually milder than observed here, and prolonged bleeding time is less common [2]. *Scrub typhus* - Caused by Orientia tsutsugamushi, it is characterized by **fever, headache, myalgia, and a characteristic eschar** (necrotic ulcer) at the bite site, which is not mentioned. - While it can cause rash and some thrombocytopenia, the **petechial rash** and such severe thrombocytopenia with prolonged bleeding time are less typical. *Typhoid* - Presents with **sustained high fever**, headache, bradycardia, and sometimes a **rose spot rash** (maculopapular), which is different from a petechial rash. - Typhoid typically causes **leukopenia** and can lead to gastrointestinal complications like intestinal bleeding, but severe thrombocytopenia and extensive petechiae are not common presenting features.
Explanation: ***Chikungunya*** - **Chikungunya** is a viral disease transmitted by mosquitoes that commonly presents with **fever**, severe **joint pain** (polyarthralgia), and a **rash**, fitting the patient's symptoms. - Its high prevalence in **urban areas** and recent history of **mosquito bites** make it a strong diagnostic consideration. *Dengue* - While Dengue also causes **fever** [1] and a **rash**, it is more typically associated with **severe muscle and bone pain** ("breakbone fever"), and **hemorrhagic manifestations** or shock, which are not mentioned. - **Joint pain** in dengue is usually less debilitating than in chikungunya. *Japanese Encephalitis* - This is a serious **neurological infection** characterized by **fever**, **headache**, seizures, and altered mental status, rather than prominent joint pain and rash. - It primarily affects the **brain** and is less likely to present with this specific symptom triad. *Malaria* - Malaria is characterized by **cyclic fevers**, chills, sweating, and fatigue, but typically **does not present with a rash** [1] or significant joint pain. - It is caused by a **parasite** transmitted by *Anopheles* mosquitoes, and its clinical picture differs from the described symptoms.
Explanation: ***P. falciparum*** - **Recrudescence** refers to the reappearance of malaria symptoms after a period of remission, due to the survival and subsequent increase of asexual parasites in the blood [1]. - This is common in *P. falciparum* due to the high parasite burden and its ability to sequester in deep capillaries, evading splenic clearance and developing drug resistance. *P. vivax* - *P. vivax* is known for **relapses**, which are caused by the activation of dormant liver stages called **hypnozoites**, rather than a recrudescence of blood-stage parasites [1]. - Relapses can occur months or years after the initial infection, even after the blood-stage parasites have been cleared. *P. malariae* - *P. malariae* is uniquely characterized by infections that can persist for many years, even decades, causing symptoms of **recrudescence**, although less frequently than *P. falciparum* [1]. - It has a prolonged erythrocytic cycle, which can lead to chronic low-level parasitemia and sporadic symptomatic episodes. *P. ovale* - Similar to *P. vivax*, *P. ovale* also causes **relapses** due to the presence of **hypnozoites** in the liver [1]. - While it can manifest with symptoms similar to *P. vivax*, it is generally less common and causes milder disease.
Explanation: ***Idiopathic thrombocytopenic purpura (ITP)*** - This presentation, especially in a previously healthy child with a preceding viral infection 1-4 weeks prior, is highly characteristic of **acute ITP**, leading to **purpuric rash** (red spots). - The preceding viral infection often triggers an autoimmune response causing destruction of **platelets**, resulting in **thrombocytopenia**. *Dengue fever* - Dengue fever typically presents with **acute onset of fever**, **headache**, **myalgia**, and a rash that appears 3-4 days after fever onset, often with a shorter incubation period than 1-4 weeks. - While it can cause petechiae due to **thrombocytopenia**, the symptom constellation does not perfectly align with the scenario, particularly the sudden onset of spots without mention of fever or other acute symptoms. *Hemophilia A* - **Hemophilia A** is a **hereditary bleeding disorder** causing deficits in **Factor VIII**, leading to spontaneous bleeding into joints and muscles, and prolonged bleeding after trauma. - It does not present as sudden onset red spots (petechiae/purpura) following a viral infection but rather as larger **hematomas** or **hemarthroses**, and it's a chronic condition, not typically triggered by recent infection. *Thrombotic thrombocytopenic purpura (TTP)* - TTP is characterized by the **pentad of symptoms**: **fever**, **neurological symptoms**, **renal dysfunction**, **microangiopathic hemolytic anemia**, and **thrombocytopenia**. - While it involves thrombocytopenia and can cause purpura, the patient's presentation lacks the other severe systemic features typically associated with TTP, and it's less commonly triggered by a simple viral infection in children.
Explanation: ***Correct: Jaswant Singh Bhattacharya (JSB) Stain is used.*** - **JSB stain** is a rapid and effective method for staining malaria parasites in blood films, particularly in resource-limited settings where traditional Romanowsky stains might not be readily available. - Its quick staining time (3-5 minutes) and ease of use make it valuable for prompt diagnosis of malaria. - This is the **most clearly correct** statement as JSB stain is definitively used in malaria diagnosis. *Thick blood film is used to detect plasmodium species causing infection.* - A **thick blood film** is primarily used for **detecting** the presence of malaria parasites due to its higher sensitivity in screening larger volumes of blood (concentrates parasites 20-40 times). - However, it is **not ideal for species identification** due to distorted RBC morphology and lysed red blood cells. - The statement is **misleading** - while thick films detect parasites, they are not the preferred method for determining the **specific species**. *Thin blood film is used to determine parasite concentration.* - This statement is **technically correct** - thin blood films ARE used to determine parasite concentration (parasitemia) and for speciation. - However, in the context of this question, **JSB stain is the better answer** as it is more specifically and uniquely associated with malaria diagnosis, whereas thin films have broader applications. - Thin films allow accurate quantification of parasitemia (parasites/µL or percentage of infected RBCs) and species identification due to preserved RBC morphology. *As the sensitivity of microscopy is low, it is useful to detect parasite load at high concentrations only.* - **Incorrect** - Microscopy, particularly with thick blood films, has **high sensitivity** and is considered the gold standard for malaria diagnosis. - Microscopy can detect parasites at concentrations as low as **50-100 parasites/µL** (approximately 0.001% parasitemia). - While operator-dependent, it is certainly not limited to detecting parasites only at high concentrations.
Explanation: ***Erythema nodosum*** - Erythema nodosum is a common **cutaneous adverse drug reaction** to anti-TB medications, presenting with **tender, erythematous nodules** typically on the shins. - It is a form of **panniculitis** (inflammation of subcutaneous fat) specifically associated with various triggers, including infections and drugs, making it highly probable in this context. *Sweet syndrome* - Sweet syndrome (acute febrile neutrophilic dermatosis) presents with **tender, erythematous plaques and nodules** often associated with fever and leukocytosis. - While it can be drug-induced, it typically involves a more widespread skin eruption and prominent systemic symptoms like **fever**, which are not specified here. *Panniculitis* - Panniculitis is a general term for **inflammation of the subcutaneous fat**, and erythema nodosum is a type of panniculitis. - This option is too broad; while accurate, "Erythema nodosum" is the **most specific and likely diagnosis** given the patient’s presentation in the context of anti-TB drug use. *Erythema multiforme* - Erythema multiforme is characterized by **target lesions** (concentric rings of erythema and edema) and often involves mucous membranes. - The description of **tender nodules on shins** does not fit the characteristic morphology of erythema multiforme.
Explanation: ***Nickel*** - **Nickel** is the most frequent cause of **allergic contact dermatitis**, commonly found in jewelry, belt buckles, and zippers. - Exposure leads to a **Type IV hypersensitivity reaction**, characterized by erythema, itching, and vesiculation. *Gold* - While gold can cause contact dermatitis, it is **far less common** than nickel allergy. - Reactions to gold are often seen with prolonged skin contact, such as with jewelry. *Silver* - **Silver** is a **rare cause** of allergic contact dermatitis. - Allergic reactions to silver are typically observed in individuals with extensive exposure, such as jewelers. *Iron* - **Iron** is **not a common precipitant** of contact dermatitis. - Allergic reactions to iron are exceedingly rare, as iron is an essential element found naturally in the body.
Explanation: ***Antibiotics*** - **Antibiotics**, particularly **sulfonamides** (e.g., sulfamethoxazole-trimethoprim) and **beta-lactams** (e.g., penicillins, cephalosporins), are among the most common drug classes implicated in causing **Stevens-Johnson Syndrome (SJS)**. - SJS is a severe **idiosyncratic drug reaction**, and many antibiotics can trigger this immune-mediated response. - **Note:** Other major causative drug classes include **anticonvulsants** (carbamazepine, phenytoin, lamotrigine), **allopurinol**, and **NSAIDs**, but among the options listed, antibiotics are the most commonly implicated. *Corticosteroids* - **Corticosteroids** are typically used in the **treatment** of SJS to suppress the immune response and reduce inflammation, not to cause it. - While they have their own set of side effects, initiating SJS is not one of their known adverse reactions. *Antifungals* - Although some **antifungals** can cause adverse drug reactions, they are **not typically associated** with SJS compared to antibiotics, anticonvulsants, or allopurinol. - The risk of SJS with antifungal medications is generally very low. *Proton pump inhibitors* - **Proton pump inhibitors (PPIs)** are generally well-tolerated and are **rarely implicated** as a cause of SJS. - Their primary side effects are usually gastrointestinal and not severe dermatological reactions.
Explanation: ***Cold temperature*** - **Cutis marmorata** is a physiological response to **cold temperatures**, characterized by a mottled, reticulated vascular pattern on the skin. - This occurs due to **vasoconstriction** of the small arteries and arterioles, alongside **vasodilation** of the venules, creating the characteristic marbled appearance. *Dust* - Exposure to **dust** typically causes **irritation**, allergic reactions, or respiratory issues, such as **dermatitis**, **contact urticaria**, or **asthma**. - It does not directly lead to the characteristic vascular changes seen in cutis marmorata. *Hot temperature* - **Hot temperatures** generally cause **vasodilation** in the skin to facilitate **heat dissipation**, leading to redness and warmth. - This is the opposite physiological response to cutis marmorata, which involves vasoconstriction. *Humidity* - **Humidity** primarily affects **skin hydration** and the rate of perspiration, potentially exacerbating certain skin conditions like **eczema** or **fungal infections**. - High or low humidity does not directly induce the vascular changes that result in cutis marmorata.
Explanation: **Explanation:** **Lymphogranuloma venereum (LGV)** is caused by the **L1, L2, and L3 serovars of *Chlamydia trachomatis***. The "Sign of the Groove" (Greenblatt’s sign) is a pathognomonic clinical finding in the secondary stage of LGV. It occurs when the inguinal and femoral lymph nodes enlarge simultaneously, separated by the rigid **inguinal ligament**. This creates a visible depression or "groove" between the two groups of inflamed lymph nodes. **Analysis of Incorrect Options:** * **B. Granuloma Inguinale (Donovanosis):** Caused by *Klebsiella granulomatis*. It presents with painless, beefy-red, velvety ulcers. It is characterized by "pseudobuboes" (subcutaneous granulation tissue) rather than true lymphadenopathy. * **C. Syphilis:** Primary syphilis presents with a painless, indurated "hard chancre." While it causes bilateral inguinal lymphadenopathy, the nodes are discrete, rubbery, and do not form a groove. * **D. Chancroid:** Caused by *Haemophilus ducreyi*. It presents with painful, soft ulcers and painful inflammatory buboes that are usually unilateral and may suppurate, but they do not form the characteristic groove sign. **High-Yield Clinical Pearls for NEET-PG:** * **Stages of LGV:** Primary (painless papule/ulcer), Secondary (Inguinal syndrome with the Groove sign), and Tertiary (Genito-anorectal syndrome/Elephantiasis). * **Diagnosis:** Frei test (historical), NAAT (current gold standard), and **Donovan bodies** (safety-pin appearance) are seen in Donovanosis, NOT LGV. * **Treatment:** Doxycycline (100 mg BID for 21 days) is the drug of choice for LGV.
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