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Granulomatous disorders
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Part 2 book "Textbook of oral medicine, oral diagnosis and oral radiology" includes content: Dental caries, pulp and periapical lesions; gingival and periodontal diseases; regressive alterations of teeth; systemic disorders and their clinical implications; bone diseases and fibro osseous lesions; autoimmune disorders; granulomatous diseases; sexually transmitted diseases; nutritional and metabolic disorders;.... and other contents.
495p
muasambanhan10
06-04-2024
6
2
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Part 3 book "Blackwell's five minute veterinary consult clinical companion - Small animal dermatology" includes content: Otitis externa, media, and interna; panniculitis; photodermatoses; pododermatitis and claw disorders; pre and paraneoplastic syndromes; sarcoptid mites; sebaceous adenitis, granulomatous; sporotrichosis; superficial necrolytic dermatitis; tumors, common skin and hair follicle; uveodermatologic syndrome; vasculitis. viral dermatoses, zoonosis.
312p
oursky08
01-11-2023
4
2
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Part 2 book "Hair loss disorders in domestic animals" includes content: Congenital alopecia, trichomalacia, disorders of hair follicle cycling, hair follicle dystrophy and atrophy, traumatic alopecia, scarring alopecia, folliculitis with intraluminal organisms; eosinophilic folliculitis; pustular folliculitis; lymphocytic mural folliculitis; histiocytic or granulomatous mural folliculitis; necrotizing mural folliculitis; alopecia areata; sebaceous adenitis.
158p
oursky08
01-11-2023
3
3
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Sarcoidosis is a benign systemic granulomatous disorder of unknown etiology. Cell-mediated immunity disorder is often found in sarcoidosis patients, and an association between malignant tumors and sarcoidosis has been suggested.
7p
vigamora
23-05-2023
6
2
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Childhood sarcoidosis is characterized by arthritis, uveitis, and cutaneous involvement. Glucocorticoids remain the first choice therapy for children with multisystem involvement. The prognosis of early-onset childhood sarcoidosis varies in different studies due to the rarity of the disease.
5p
inception36
30-11-2021
9
1
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Hermansky-Pudlak syndrome (HPS) is an autosomal recessive disorder that is associated with oculocutaneous albinism, bleeding diathesis, granulomatous colitis, and highly penetrant pulmonary fibrosis in some subtypes.
6p
vimaine2711
26-03-2021
11
1
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Actinomycosis is a rare, chronic granulomatous disease caused by Gram-positive anaerobic bacteria that colonize the oral cavity. Cervicofacial actinomycosis is the most frequent clinical presentation of actinomycosis, but hematogenous osteomyelitis at distant sites can occur in rare instance in immunocompromised or pediatric patients, only a few cases have been reported in healthy patients.
8p
vivermont2711
28-01-2021
7
2
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Chronic granulomatous disease is a rare inherited disorder of the innate immune system. In patients with a clinical history of recurrent or persistent infections, especially infections caused by uncommon species, chronic granulomatous disease should be considered.
4p
vichengshin2711
29-02-2020
9
1
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(BQ) Continued part 1, part 2 of the document Handbook of self assessment and review ENT has contents: Granulomatous disorders of nose, nasal polyps and foreign body in nose, inflammatory disorders of nasal cavity, oral cavity, anatomy of pharynx, tonsils and adenoids, pharynx hot topics,... and other contents. Invite you to refer.
240p
thuongdanguyetan06
06-06-2019
19
1
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part 1 book "self assessment and review ent" has contents: anatomy of ear, assessment of hearing loss, lesion of cerebellopontine angle and acoustic neuroma, rehabilitative methods, glomus tumor and other tumors of the ear, anatomy and physiology of nose,... and other contents.
217p
tieu_vu13
06-08-2018
29
1
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part 2 book "self assessment and review ent" has contents: granulomatous disorders of nose, nasal polyps and foreign body in nose, granulomatous disorders of nose, nasal polyps and foreign body in nose, anatomy of pharynx, tonsils and adenoids, pharynx hot topics, lesions of nasopharynx and hypopharynx including tumors of pharyn,... and other contents.
240p
tieu_vu13
06-08-2018
31
1
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(bq) part 1 book "treatment for skin color" presents the following contents: acneiform disorders, bullous and pustular disorders, collagen vascular diseases, eczematous disorders, granulomatous disorders, hypersensitivity and allergic disorders, infectious diseases,...
201p
thangnamvoiva5
14-07-2016
48
5
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(BQ) Continued part 1, part 2 of the document Atlas and synopsis of lever's histopathology of the skin presents the following contents: Perivascular, diffuse and granulomatous infiltrates of the reticular dennis; erivascular, diffuse and granulomatous infiltrates of the reticular dennis; inflammatory and other benign disorders of skin appendages; disorders of the subcutis.
323p
thangnamvoiva3
01-07-2016
56
4
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Tuberculosis and sarcoidosis are chronic diseases that rarely occur concomitantly. Sarcoidosis is a multisystem granulomatous disorder characterized pathologically by the presence of non-caseating granulomas in involved tissues. Tuberculosis is infectious disease caused by Mycobacterium tuberculosis characterized by granulomas with caseous necrosis. Case presentation: We present a case of 43-year-old female refugee from Kosovo with microbiological confirmation of pulmonary tuberculosis and pulmonary and skin sarcoidosis at the same time.
5p
taisaocothedung
12-01-2013
44
3
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Disorders of the Mononuclear Phagocyte System Many disorders of neutrophils extend to mononuclear phagocytes. Thus, drugs that suppress neutrophil production in the bone marrow can cause monocytopenia. Transient monocytopenia occurs after stress or glucocorticoid administration. Monocytosis is associated with tuberculosis, brucellosis, subacute bacterial endocarditis, Rocky Mountain spotted fever, malaria, and visceral leishmaniasis (kala azar).
6p
konheokonmummim
03-12-2010
65
4
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Chronic Granulomatous Disease Chronic granulomatous disease (CGD) is a group of disorders of granulocyte and monocyte oxidative metabolism. Although CGD is rare, with an incidence of 1 in 200,000 individuals, it is an important model of defective neutrophil oxidative metabolism. Most often CGD is inherited as an X-linked recessive trait; 30% of patients inherit the disease in an autosomal recessive pattern. Mutations in the genes for the four proteins that assemble at the plasma membrane account for all patients with CGD.
5p
konheokonmummim
03-12-2010
94
4
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Table 47-1 Causes of Hypercalcemia Excessive PTH production Primary hyperparathyroidism (adenoma, hyperplasia, rarely carcinoma) Tertiary hyperparathyroidism (long-term stimulation of PTH secretion in renal insufficiency) Ectopic PTH secretion (very rare) Inactivating mutations in the CaSR (FHH) Alterations in CaSR function (lithium therapy) Hypercalcemia of malignancy Overproduction of PTHrP (many solid tumors) Lytic skeletal metastases (breast, myeloma) Excessive 1,25(OH)2D production Granulomatous diseases (sarcoidosis, tuberculosis, silicosis) Lymphomas Vitamin D intoxic...
5p
ongxaemnumber1
29-11-2010
65
2
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