Scott C. Howard

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Scott C. Howard

Scott C. Howard

@schowardjd

Law | Medicine | @UF #GoGators, @GWAlumni, inter alia | 𝕏 ≠ legal/medical advice | Scientia quaesitor

United States 加入时间 Ocak 2009
5.8K 关注11.1K 粉丝
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Scott C. Howard
Scott C. Howard@schowardjd·
A 21-month-old boy w/ recently diagnosed trisomy 21 & asthma presented w/ a 6-month hx of an asymptomatic, progressively enlarging plaque on the extensor left arm. There was no preceding trauma, friction, pruritus, pain, or constitutional symptoms. FMHx was notable for trisomy 21 in two distant relatives. O/E: a solitary, well-circumscribed, firm, oval yellow-brown to brown plaque measuring 2–3 cm on the extensor left arm, w/ a mildly verrucous/wrinkled surface & irregular borders. No scale, crusting, or ulceration was present. Dermoscopy demonstrated a hypopigmented center with peripheral brown pigmentation & fine linear vessels. Darier sign was -ve. CBC, CMP, & lipid profile were unremarkable. What’s the diagnosis❔
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Scott C. Howard
Scott C. Howard@schowardjd·
Japanese Spotted Fever (Rickettsia japonica) - Classic triad of rickettsial disease: Fever, rash, & an eschar (the lesion on the ankle). Mx: Start doxy empirically w/out waiting for confirmatory serology/PCR.
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Dr sthanu subramanian
Dr sthanu subramanian@drsthanus·
A woman in her 60s living in Japan presented with a 5-day history of fevers, myalgias, and petechial rash spreading on her arms, trunk, palms, and soles. A lesion on the ankle.👇 Likely diagnosis?
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Scott C. Howard
Scott C. Howard@schowardjd·
@hemo_shk Dx: Eruptive syringomas DDx: Verruca plana, sebaceous hyperplasia, angiofibromas in TSC (less likely)
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Scott C. Howard
Scott C. Howard@schowardjd·
A man in his 20s presents w/ several-mo hx of a slowly progressive, pruritic lesion on the malleolar/ankle region. Exam shows a well-demarcated hyperkeratotic, lichenified verrucous plaque w/surface thickening & excoriations from chronic scratching. What’s the diagnosis❔
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Dr Amin
Dr Amin@Naa__cheez·
@schowardjd Hypertrophic Lichen Planus With Wickham striae
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🌺SoZ🌺
🌺SoZ🌺@SHEROZTRK·
@schowardjd Let us take a moment for the one who creates healing and His healers on the earth! You guys are great!
GIF
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Scott C. Howard
Scott C. Howard@schowardjd·
A man in his late 60s presented with a febrile prodrome of high fever & sore throat followed by the acute onset of erythematous plaques, tense bullae, & oral mucosal erosions involving the trunk & extremities. He denied recent medication exposure, including antibiotics & NSAIDs. O/E: erosions of the oral & nasal mucosa w/ hemorrhagic crusting of the lips and eyelids, without conjunctival involvement. Annular erythematous plaques & bullae were distributed over the trunk, extremities, axillae, groin, palms, & soles. What’s your DDx❓
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Scott C. Howard
Scott C. Howard@schowardjd·
This is hypertrophic lichen planus. @MedicalSphereAI - Dx, DDx, W/U, Mx>
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Scott C. Howard
Scott C. Howard@schowardjd·
@SHEROZTRK Fortunately, following corticosteroid pulse therapy, the patient improved rapidly & remains relapse-free. 🎉
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Scott C. Howard
Scott C. Howard@schowardjd·
Herpes zoster (shingles) T9-T10 dermatomes Tx options: acyclovir, valacyclovir, or famciclovir. Consider pregabalin, gabapentin, or amitriptyline +/- lidocaine patches for acute herpetic neuralgia. Etiology: reactivation of the varicella-zoster virus @RoshReview>
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Keith Siau
Keith Siau@drkeithsiau·
If you saw this in a patient with ulcerative colitis, what diagnosis would you consider?
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Scott C. Howard
Scott C. Howard@schowardjd·
A man in his 20s presented with erythematous, scaly plaques confined to sharply demarcated depigmented patches. The lesions demonstrated a striking pattern of colocalization. What are the two diagnoses❔
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Scott C. Howard
Scott C. Howard@schowardjd·
A woman in her 60s presented w/ a several-wk hx of eruptive asymptomatic blanchable vascular papules on the face, chest, back, & UEs. She denied pruritus, pain, bleeding, or systemic sx. O/E: numerous lesions composed of a central erythematous papule w/ radiating telangiectasias. No jaundice, palmar erythema, ascites, hepatomegaly, or other stigmata of CLD. PMH -ve for liver dz, EtOH misuse, pregnancy, estrogen use, endocrinopathy, CTD, or hereditary vascular syndromes. She has been taking a CCB for HTN x10 yrs. CBC, CMP, LFTs, coagulation studies, thyroid/hormonal testing, & imaging were unremarkable. What’s the diagnosis❓
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Scott C. Howard
Scott C. Howard@schowardjd·
@Beshokhaton8 Poikiloderma of Civatte involves reticulated erythema, pigmentation, & atrophy from sun exposure on the neck & chest, unlike the discrete spider-like vascular papules shown here... These are spider angiomas.
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Scott C. Howard
Scott C. Howard@schowardjd·
These eruptive, asymptomatic, blanchable vascular papules diffusely involving the face, trunk, & upper extremities, each w/ a central arteriole & radiating telangiectasias, are consistent w/ spider angiomas. No clinical, laboratory, or imaging evidence of hepatic disease, hyperestrogenism, endocrine abnormality, or systemic vascular disorder. Given the absence of classic etiologies, this represents diffuse eruptive spider angiomas, associated with long-term dihydropyridine calcium-channel blocker therapy. Mx involved discontinuation of the suspected offending agent in coordination with cardiology, followed by treatment with 1064-nm long-pulsed Nd:YAG laser, resulting in marked clinical regression of lesions on follow-up.
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Scott C. Howard@schowardjd

A woman in her 60s presented w/ a several-wk hx of eruptive asymptomatic blanchable vascular papules on the face, chest, back, & UEs. She denied pruritus, pain, bleeding, or systemic sx. O/E: numerous lesions composed of a central erythematous papule w/ radiating telangiectasias. No jaundice, palmar erythema, ascites, hepatomegaly, or other stigmata of CLD. PMH -ve for liver dz, EtOH misuse, pregnancy, estrogen use, endocrinopathy, CTD, or hereditary vascular syndromes. She has been taking a CCB for HTN x10 yrs. CBC, CMP, LFTs, coagulation studies, thyroid/hormonal testing, & imaging were unremarkable. What’s the diagnosis❓

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Scott C. Howard
Scott C. Howard@schowardjd·
This is systemic AL (light-chain) amyloidosis presenting w/ the uncommon combination of bullous amyloidosis, dyschromia, & macroglossia. Biopsies from both a bulla & a pigmented lesion demonstrated dermal amyloid deposition with Congo red positivity, while tongue biopsy confirmed amyloid infiltration with characteristic apple-green birefringence under polarized light. Further evaluation revealed a marked lambda free light-chain excess, an abnormal κ:λ ratio, and a clonal plasma-cell infiltrate on bone marrow biopsy, establishing the diagnosis of AL amyloidosis secondary to an underlying plasma-cell dyscrasia. Cardiac studies also suggested early amyloid involvement. Although cutaneous AL amyloidosis most commonly presents w/ purpura & waxy papules, bullous lesions are a rare manifestation & may mimic bullous pemphigoid, diabetic bullae, or edema blisters. The presence of progressive macroglossia, hoarseness, fatigue, & characteristic mucocutaneous findings should prompt evaluation for systemic amyloidosis. The patient was treated with daratumumab, cyclophosphamide, bortezomib, & dexamethasone, resulting in stabilization of the bullous eruption and improvement in macroglossia.
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Scott C. Howard
Scott C. Howard@schowardjd·
A woman in her late 60s w/ T2DM, hypothyroidism, HTN, & dyslipidemia presented w/ a 1-year hx of asymptomatic lower-extremity bullae. Exam revealed tense bullae arising on a background of mottled hyper- and hypopigmented patches, hemorrhagic crusts, & excoriations on both legs. She also reported a 4-month hx of progressive fatigue, hoarseness, & tongue enlargement causing difficulty eating & breathing. Oral exam demonstrated marked macroglossia w/ a rubbery, scalloped tongue. What’s the diagnosis❔
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